CN1780731A - Dry paint transfer laminate. - Google Patents
Dry paint transfer laminate. Download PDFInfo
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- CN1780731A CN1780731A CNA200480009775XA CN200480009775A CN1780731A CN 1780731 A CN1780731 A CN 1780731A CN A200480009775X A CNA200480009775X A CN A200480009775XA CN 200480009775 A CN200480009775 A CN 200480009775A CN 1780731 A CN1780731 A CN 1780731A
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- Prior art keywords
- dry
- release
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- coated bed
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
- B32B7/04—Interconnection of layers
- B32B7/06—Interconnection of layers permitting easy separation
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
- B32B27/20—Layered products comprising a layer of synthetic resin characterised by the use of special additives using fillers, pigments, thixotroping agents
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B37/00—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding
- B32B37/14—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the properties of the layers
- B32B37/15—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the properties of the layers with at least one layer being manufactured and immediately laminated before reaching its stable state, e.g. in which a layer is extruded and laminated while in semi-molten state
- B32B37/153—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the properties of the layers with at least one layer being manufactured and immediately laminated before reaching its stable state, e.g. in which a layer is extruded and laminated while in semi-molten state at least one layer is extruded and immediately laminated while in semi-molten state
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B44—DECORATIVE ARTS
- B44C—PRODUCING DECORATIVE EFFECTS; MOSAICS; TARSIA WORK; PAPERHANGING
- B44C1/00—Processes, not specifically provided for elsewhere, for producing decorative surface effects
- B44C1/16—Processes, not specifically provided for elsewhere, for producing decorative surface effects for applying transfer pictures or the like
- B44C1/165—Processes, not specifically provided for elsewhere, for producing decorative surface effects for applying transfer pictures or the like for decalcomanias; sheet material therefor
- B44C1/17—Dry transfer
- B44C1/1712—Decalcomanias applied under heat and pressure, e.g. provided with a heat activable adhesive
- B44C1/1716—Decalcomanias provided with a particular decorative layer, e.g. specially adapted to allow the formation of a metallic or dyestuff layer on a substrate unsuitable for direct deposition
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B44—DECORATIVE ARTS
- B44C—PRODUCING DECORATIVE EFFECTS; MOSAICS; TARSIA WORK; PAPERHANGING
- B44C1/00—Processes, not specifically provided for elsewhere, for producing decorative surface effects
- B44C1/16—Processes, not specifically provided for elsewhere, for producing decorative surface effects for applying transfer pictures or the like
- B44C1/165—Processes, not specifically provided for elsewhere, for producing decorative surface effects for applying transfer pictures or the like for decalcomanias; sheet material therefor
- B44C1/17—Dry transfer
- B44C1/1733—Decalcomanias applied under pressure only, e.g. provided with a pressure sensitive adhesive
- B44C1/1737—Decalcomanias provided with a particular decorative layer, e.g. specially adapted to allow the formation of a metallic or dyestuff on a substrate unsuitable for direct deposition
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B44—DECORATIVE ARTS
- B44C—PRODUCING DECORATIVE EFFECTS; MOSAICS; TARSIA WORK; PAPERHANGING
- B44C7/00—Paperhanging
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/20—Adhesives in the form of films or foils characterised by their carriers
- C09J7/22—Plastics; Metallised plastics
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/40—Properties of the layers or laminate having particular optical properties
- B32B2307/402—Coloured
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2309/00—Parameters for the laminating or treatment process; Apparatus details
- B32B2309/08—Dimensions, e.g. volume
- B32B2309/10—Dimensions, e.g. volume linear, e.g. length, distance, width
- B32B2309/105—Thickness
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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- Y10S428/906—Roll or coil
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- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T156/00—Adhesive bonding and miscellaneous chemical manufacture
- Y10T156/11—Methods of delaminating, per se; i.e., separating at bonding face
- Y10T156/1168—Gripping and pulling work apart during delaminating
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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- Y10T428/1405—Capsule or particulate matter containing [e.g., sphere, flake, microballoon, etc.]
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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- Y10T428/1452—Polymer derived only from ethylenically unsaturated monomer
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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- Y10T428/1462—Polymer derived from material having at least one acrylic or alkacrylic group or the nitrile or amide derivative thereof [e.g., acrylamide, acrylate ester, etc.]
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- Y10T428/1486—Ornamental, decorative, pattern, or indicia
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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- Y10T428/24355—Continuous and nonuniform or irregular surface on layer or component [e.g., roofing, etc.]
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- Y10T428/24802—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.]
- Y10T428/24851—Intermediate layer is discontinuous or differential
- Y10T428/2486—Intermediate layer is discontinuous or differential with outer strippable or release layer
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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- Y10T428/24851—Intermediate layer is discontinuous or differential
- Y10T428/24868—Translucent outer layer
- Y10T428/24876—Intermediate layer contains particulate material [e.g., pigment, etc.]
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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- Y10T428/28—Web or sheet containing structurally defined element or component and having an adhesive outermost layer
- Y10T428/2848—Three or more layers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Laminated Bodies (AREA)
- Adhesive Tapes (AREA)
- Paints Or Removers (AREA)
Abstract
The disclosed invention relates to a dry coating transfer (or multi-layer) lamination material (100) which comprises a dry coating layer (110) which comprises a color layer which is provided with base material and paint, wherein the dry coating layer (110) is provided with an upper surface (112) and a lower surface (114), a pressure sensitive adhesive layer (120) which covers the upper surface (112) of the dry coating layer (110) and a release pad (130) which is used to cover the lower surface (114) of the dry coating layer (110). The release pad (130) comprises a first coating layer (or a load release coating or a rough surface release coating) (135), and the first coating layer comprises particles which can enter into the surface (114) of the dry coating layer (110), the particles are used to transfer the rough surface release coating to the surface (114) when the pressure sensitive adhesive layer (120) adheres the lamination material (100) to a base under the condition of exerting pressure and the release pad (130) is stripped off from the dry coating layer (110).
Description
Technical field
The present invention relates to dry-coated material transfer laminate (dry paint transfer laminates).These laminated materials are layer laminates, it comprises the dry-coated bed of material (dry paint layer), cover the adhesive layer (adhesive layer) of a side of the dry-coated bed of material and cover the release liner (release liner) of the opposite side of the dry-coated bed of material.
Background of invention
Use the tradition japanning process of liquid coating must need number step preparation process, comprise hiding not coated portion and spreading protection cloth (drop cloths).Traditional japanning process also must be carried out the cleaning of trouble to hairbrush, roller and analog, also can run into and spill problem, is exposed to flue gas, and because of coating drying time delay.When the expectation special-effect is covered with paint, lacquer, colour wash, etc. (faux finishes) such as the simulation wood grain, also need extra time and effort to coat extra coating.
The invention provides a scheme at these problems.Adopt the present invention, do not need to hide not coated portion, and also do not need to use protection cloth (drop cloth).Irksome cleaning at hairbrush, roller and analog is avoided.Spilling the problem of spattering and being exposed to flue gas is avoided.Because of waiting for that the coating drying is also avoided time delay.Special effect is for example simulated wood grain and is covered with paint, lacquer, colour wash, etc. finishing of (faux finishes) and can be realized by single covering with paint once.
The invention summary
The present invention relates to a kind of dry-coated material transfer laminate (dry paint transfer laminate), comprise: the dry-coated bed of material (dry paint layer), it contains color layers, and color layers comprises base-material and pigment, and this dry-coated bed of material has upper surface and lower surface; Dry-pressing sensitive adhesive layer (drypressure-sensitive adhesive layer) covers the upper surface of the described dry-coated bed of material; And release liner (release liner), adhere to releasedly on the lower surface of the described dry-coated bed of material, described release liner has the carrying release coat, wherein contain and protrude the particle that enters into the dry-coated bed of material that adheres to releasedly, be used for coarse facing (matte finish) is transferred to the exposed surface of the described dry-coated bed of material, adhering to laminated material in the substrate under pressure when adhesive layer and release liner is peeled off from the dry-coated bed of material and taken place when going to shift.
In one embodiment, release liner further comprises: the adhesive release coat, be positioned at a side of liner, and be to be in and the relative side of carrying release coat.
In one embodiment, the dry-coated bed of material contains hyaline layer, and between the color layers and release liner of the dry-coated bed of material, and therein, the carrying release coat is to adhere on the hyaline layer releasedly.
In one embodiment, the present invention relates to a kind of dry-coated material transfer laminate, comprising: the dry-coated bed of material, it contains the color layers that comprises base-material and pigment and is positioned at hyaline layer on the color layers; Dry-pressing sensitive adhesive layer is positioned on the surface of the dry-coated bed of material, is on the side dry-coated bed of material, relative with hyaline layer; And release liner, contact with the surface of the dry-coated bed of material releasedly, be in and the adhesive opposite face; Described release liner has dried matsurface release coat (dry matterelease coat layer), bond with release liner, and comprise the particle that contacts with hyaline layer, like this, when applying pressure to adhesive layer so that adhere to laminated material to substrate, thereafter, thus release liner exposes the rough surface of hyaline layer from discharging with dry-coated bed of material contact condition of it, will produce the unglazed smooth or surperficial facing of semi-glossy on the exposed surface of hyaline layer.
In one embodiment, the present invention relates to a kind of dry-coated material transfer laminate, comprising: the matsurface release liner, it contains soft polymer carrier film and discharges overlay with the dried matsurface that is bonded on the described carrier film; The soft dry-coated bed of material discharges overlay with matsurface on release liner releasedly and contacts; With dried adhesive layer, be bonded to the dry-coated bed of material, side with matsurface release liner position opposite, the described dry-coated bed of material (dry paint layer) comprises the pigment that is dispersed in the polymer base material, described matsurface discharges overlay and has the adherence (tack) of certain level, when with adhesive one side of laminated material as for substrate state of contact following time, it adheres to the matsurface release liner on the dry-coated bed of material releasedly, thereby for laminated material provides support, described adhesive layer comprises pressure-sensitive adhesive, by applying pressure on the dry-coated material transfer laminate, be used for the dry-coated bed of material is adhered to substrate, described matsurface release coat comprises particle, particle protrudes and enters the dry-coated bed of material, like this, after laminated material had adhered in the substrate already, release liner just is used in coarse facing is transferred on the exposed surface of the described dry-coated bed of material by from discharging the dry-coated bed of material contacts.
In one embodiment, release liner comprises the matsurface release coat that is made by thermoset resin material on thin and soft polymerization carrier film and the carrier film, and matsurface release coat and carrier film bonding also form rough surface; When at ambient temperature, when the dry-coated bed of material removed release liner, rough surface facing (matte surface finish) was just transferred on the dry-coated bed of material.
In one embodiment, release liner comprises the matsurface release coat that contacts with dry-coated bed of material tiling on thin and soft polymerization carrier film and the carrier film, the matsurface release coat is made by the resinous coat material that is the attitude of hardening under the room temperature, wherein coating material (1) forms the rough surface that is releasably attached to the dry-coated bed of material, (2) at ambient temperature, discharge from dry-coated bed of material surface, (3) when release liner by when the dry-coated bed of material removes, the transferring rough surface facing is to the exposed surface of the described dry-coated bed of material.
In one embodiment, the present invention relates to a kind of layer laminates, comprising: release liner, the matsurface release coat that has soft polymer carrier film and bond with carrier film; Soft dry-coated material transfer layer is releasably attached on the matsurface release coat; With dry-pressing sensitive adhesive layer,, be in a relative side with the position of release liner with dry-coated material transfer layer one side bonding; Described dry-coated material transfer layer contains color layers, and color layers comprises the pigment that is included in the polymer base material; Described matsurface discharges overlay and has certain adherence, and when adhesive one side of placing the dry-coated bed of material contacted with substrate, it preferentially adhered to release liner to dry-coated material transfer layer, is enough to provide for the dry-coated bed of material structural support of certain level; Described matsurface release coat comprises the resin material that hardens or be solidified to form the micro-rough surface, when release coat and the dry-coated bed of material disengage, is used for the rough surface form is transferred to the exposed surface of the dry-coated bed of material like this; Described adhesive layer at room temperature has the adherence of downtrod base level, this permission, after the dry-coated bed of material is removed release liner, laminated material is adhered in the substrate, then, because through the sufficiently long time, described adhesive layer experience the follow-up of adhesive effect gathered, make the dry-coated bed of material and substrate (substrate) permanent bond.
In one embodiment, the gloss level of transferring to the dry-coated bed of material from the matsurface release coat under 85 ° less than 30%.
In one embodiment, dry-coated material transfer layer contains clear coating layer (clear coat layer), cover on the color layers, and therein, clear coating layer contacts with the matsurface release coat, to shift the micro-rough surface to clear coating layer.
In one embodiment, release liner comprises polyester film, and it is non-ductility at ambient temperature basically.
In one embodiment, laminated material contains the reinforcement polymer support layer that is between the dry-coated bed of material and the adhesive layer, and this supporting layer has the tensile strength greater than the dry-coated bed of material.
In one embodiment, laminated material is from roll form (self-wound form), therein, separate the necessary release force of matsurface release coat (releaseforce) greater than the necessary release force of separation gel stick release coat from formation of pressure-sensitive adhesive layer from the dry-coated bed of material.
In one embodiment, matsurface discharges overlay and has the adherence of certain level, when adhesive one side that makes the dry-coated bed of material and substrate were in contact condition, this layer preferentially sticked together release liner to dry-coated material transfer layer, so that the support structure of enough levels is provided for the dry-coated bed of material; Described matsurface release coat comprises resinoid (resinous material), resinoid comprises dispersed particles shape material, wherein matsurface release coat material is hardened or is solidified, make these particles form little roughened surface, when release coat and the dry-coated bed of material disengage, be used for the rough surface form is transferred to the exposed surface of the dry-coated bed of material, the gloss level that the coarse homogeneous form of transfer has under 85 ° is less than 30%; Described adhesive layer at room temperature has downtrod initial tackness level, this makes, after the dry-coated bed of material removes release liner, allow laminated material and substrate stick together, then, because the passage of sufficiently long time, the follow-up enhancing of described adhesive layer experience adhesive effect makes the dry-coated bed of material and substrate permanent bond.
In one embodiment, the present invention relates to a kind of layer laminates, comprise what used inside, the dry-coated bed of material that comprises base-material and pigment, one of being positioned at the dry-coated bed of material is lip-deep, be used to cohere the formation of pressure-sensitive adhesive layer of the dry-coated bed of material to the body of wall, be positioned on the surface of the dry-coated bed of material, be in release liner with the adhesive layer relative position, in case the dry-coated bed of material is attached on the wall by formation of pressure-sensitive adhesive layer, described release liner can remove from the dry-coated bed of material, the described dry-coated bed of material has coarse facing (matte finish) on its exposed surface, be characterised in that: described release liner comprises thin and soft polymer carrier film and on carrier film, the matsurface release coat that contacts with dry-coated bed of material tiling, described matsurface release coat is prepared by the resin-like coating material that is the attitude of hardening under the room temperature, therein, described coating material forms rough surface, when adhesive layer sticks on the body of wall and when the dry-coated bed of material removes release liner, the rough surface facing is transferred on the exposed surface of the dry-coated bed of material, the gloss level of the described rough surface that is transferred under 85 ° is less than 30%.
In one embodiment, the present invention relates to as decorative material for internal wall, be used for the inner dry-coated material transfer laminate that uses, comprise: a dry-coated bed of material, strippingly attached on the release liner that provides support for the dry-coated bed of material, with a side that is positioned at dry coating, relative with the release liner position, be used for dope layer is adhered on the interior wall, by pressure-sensitive adhesive constitute the layer, therein, described release liner has one and can remove from the dry-coated bed of material, the dry-coated bed of material is exposed and become the release coat of the decorative material for internal wall of colouring, simultaneously, therein, described release liner is in a side of liner, on the position relative, has the adhesive release coat with the release coat of dry coating contact, be characterised in that: described release liner comprises a polymerization carrier film and the release overlay on it, release coat comprises the matsurface release coat that bonds and contact with dry coating with carrier film, described matsurface release coat is by a kind of like this material preparation, it forms little roughened surface (micro-roughened surface) of being separated by with carrier film under the sclerosis attitude, and adhesiveness with certain level, release liner is sticked on the dry-coated bed of material, but at room temperature, when adhesive layer coheres laminated material and body of wall, and when the release liner and the dry-coated bed of material disengage, coarse facing is transferred on the surface that is exposed of the dry-coated bed of material, described laminated material has from roll form, therein, be used to separate matsurface release coat and the needed release force of the dry-coated bed of material (release force) greater than the release force that is used for separation gel stick release coat and adhesive layer, described matsurface discharges the release force that overlay has certain level, be enough to remove liner and rough surface transferred on the dry coating, the coating that keeps dry simultaneously on the wall integrality and it can not discharged from its attachment state to wall.
In one embodiment, the present invention relates to a kind of method that is used to prepare layer laminates, be included in a side coating composition layer (paint layer) of release liner (release liner), and dry or coating material solidified layer (paint layer) forms dry coating (dry paintlayer) on release liner, described release liner comprises thin and soft polymer carrier film, described dope layer comprises base-material (binder) and pigment (pigment), and described release liner has the release surface (release surface) that contacts with dry coating; With a side at dope layer, with pressure-sensitive adhesive coating adhesive layer on the release liner relative position (pressure-sentitive adhensive layer), be characterised in that following step: coating matsurface release coat on release liner, described matsurface release coat comprises the resin-like thing, contain dispersed particles shape filler and at room temperature be the sclerosis attitude, it forms rough surface, the dry-coated bed of material that contacts with rough surface with the rough surface coating composition layer that discharges overlay at described matsurface and drying or curing, so that strippingly the dry-coated bed of material and rough surface are sticked together, when by formation of pressure-sensitive adhesive layer with laminated material and substrate is bonding and when removing release liner from it, described rough surface can be adjusted at ambient temperature and discharge from the dry-coated bed of material, the rough surface facing is transferred on the exposed surface of the dry-coated bed of material.
In one embodiment, the present invention relates to a kind of method for preparing dry-coated material transfer laminate, comprise: coat one or more decorative coating layers in a side of release liner, and dry or curing is positioned at the decorative coating layer on the release liner, form the dry-coated bed of material thereon, the described dry-coated bed of material contains color layers, color layers comprises base-material and pigment, the described dry-coated bed of material has upper surface and lower surface, described release liner has matsurface and discharges overlay, matsurface discharges overlay and comprises resinoid bond and dispersed particles thing, it forms the matsurface release surface on release liner, the lower surface of the described dry-coated bed of material is positioned on the matsurface release surface of release liner, strippingly contacts with it; With, formation of pressure-sensitive adhesive layer is coated onto on the upper surface of dope layer; In the time of on applying pressure to release liner, described formation of pressure-sensitive adhesive layer is suitable for the dry-coated bed of material and substrate surface are sticked together; Release liner is to discharge from the dry-coated bed of material that adheres to, and when release liner and the dry-coated bed of material disengage, can be used for coarse facing is transferred to from the matsurface release surface exposed surface of dry-coated material transfer layer.
In one embodiment, the invention is characterized in following method: on release liner, spread the matsurface release coat, described matsurface discharges overlay and at room temperature is the sclerosis attitude, make by the resin-like material, have the rough surface isolated with carrier film, with spread dope layer at rough surface, and dry or coating material solidified thereon layer, described matsurface release coat material provides the rough surface and the dry-coated bed of material has been carried out bonding bonding force, at room temperature strippingly contact with the dry-coated bed of material, when the dry-coated bed of material is bonding by formation of pressure-sensitive adhesive layer and substrate surface, so that the rough surface facing is transferred to the exposed surface of the dry-coated bed of material.
In one embodiment, the invention is characterized in following method: coating thermosetting resin matsurface release coat on release liner, and at high temperature solidify the release coat on the liner, the composition of this release coat material forms the bonding with release liner, and form the matsurface release surface that is the attitude of hardening at ambient temperature, and under its sclerosis attitude, form the adherence of certain level; With at rough surface applying coatings layer and dry or solidify dope layer on it, matsurface discharges overlay and strippingly adheres on the dry paint layer, when laminated material by formation of pressure-sensitive adhesive layer and substrate surface adhere to, release liner is thereafter by when the dry-coated bed of material is removed, at room temperature, described rough surface is transferred to the rough surface facing on the dry paint layer.
In one embodiment, the invention is characterized in following method: the coating matsurface discharges overlay on release liner, and dry thereon or curing release overlay, on liner, form rough surface, described release overlay is made by the thermosetting resin shape material that is bonded on the liner, this resin material contains the particulate material of dispersion, and it forms the rough surface on it; With at applying coatings layer on the rough surface and dry or solidify dope layer on it, when the dry-coated bed of material is bonding by formation of pressure-sensitive adhesive layer and substrate surface, by when the dry-coated bed of material is removed, transfer to the rough surface facing on the dry-coated bed of material by described rough surface thereafter for release liner.
Description of drawings
In the accompanying drawings, identical mark is represented same section or feature.
Fig. 1 is the schematic, pictorial illustration of the side view of the dry-coated material transfer laminate of an embodiment concrete form of the present invention.
Fig. 2 is the schematic, pictorial illustration of dry-coated material transfer laminate shown in Figure 1, and laminated material is partly twined into web-like.
Fig. 3 is the schematic, pictorial illustration of side view of another embodiment of dry-coated material transfer laminate of the present invention.
Fig. 4 is the schematic, pictorial illustration of side view of another embodiment of dry-coated material transfer laminate of the present invention.
Fig. 5 is the schematic, pictorial illustration of side view of another embodiment of dry-coated material transfer laminate of the present invention.
Fig. 6 is the schematic, pictorial illustration of side view of another embodiment of dry-coated material transfer laminate of the present invention.
Fig. 7 is the schematic, pictorial illustration of side view of another embodiment of dry-coated material transfer laminate of the present invention.
Fig. 8 is the schematic, pictorial illustration of side view of another embodiment of dry-coated material transfer laminate of the present invention.
Fig. 9 is the schematic, pictorial illustration of side view of another embodiment of dry-coated material transfer laminate of the present invention.
Figure 10 is the schematic, pictorial illustration of side view of another embodiment of dry-coated material transfer laminate of the present invention.
Figure 11 is the schematic, pictorial illustration of a kind of method that is used for co-extrusion pressure supporting layer and adhesive layer that adopted in the embodiment of laminated material of the present invention.
Figure 12 is the schematic, pictorial illustration of another embodiment of the method that is used for co-extrusion pressure supporting layer and adhesive layer that adopted in the embodiment of laminated material of the present invention.
Preferred embodiment is described
When relating to one deck or ground floor with respect to the concerning of another layer or the second layer, term " ... on (over) " and " cover (overlies) ", and with the etymology term as " be positioned at ... on (overlying) " and similar terms, be meant that ground floor partially or even wholly is positioned on the second layer.The ground floor that covers (overlying) second layer can contact also and can not contact the second layer.For example, one or more extra play can be placed between the ground floor and the second layer.Term " ... under side (under) " and " down lining (underlies) ", and with the etymology term as " be positioned at ... under (underlying) of side " and similar terms, have similar meaning, just ground floor partially or even wholly is positioned at the below of the second layer, but not the top.
Term " in coating (dry paint) " is meant paint composite (paint composition), and it has been used in the substrate and by sufficiently dry or solidify, and causes the user to touch or when operating, it can not defiled or make dirty.Dry paint composition (dry paintcomposition) can derive from liquid (being solvent base or water base) coating or film-forming composition, perhaps hot-melt coating or film-forming composition.In one embodiment, the dry paint composition derive from comprise one or more volatile components (as organic solvent, water, or the like) composition, wherein coating composition is implemented on the ground (substrate (substrate)), after doing to a certain degree, volatile component (volatile matter, volatile components) runs away fully or be enough to allow coating and ground bonding, and when the user touches, can not erase or make dirty.Term " volatile materials " is used to herein, and being illustrated under baking temperature and the environmental pressure is volatile material.
Term " transparent (transparent) ", in expression the present invention dry-coated material transfer laminate, when being positioned at the transparent film layer above one or more layers dry paint rete, meaning by transparent film layer and can see one or more layers dry paint rete.Transparent film layer can be translucent.
Referring to Fig. 1, the dry-coated material transfer laminate of invention in its one of the embodiment of described n-lustrative explanation, is usually indicated with reference numerals 100, and is comprised: the dry-coated bed of material or rete 110, and it has upper surface 112 and lower surface 114; Adhesive layer 120, be incumbent on the surface 112 on and with its bonding; Release liner 130, cover on the lower surface 114 and with its bonding.Release liner 130 comprises: backing pad 132 has upper surface 133 and lower surface 134; First discharges coating layer 135, on the surface 133 that is incumbent on and with its bonding; Second discharges coating layer 136, cover on the lower surface 134 and with its bonding.First discharges coating layer 135 can be called as carrying release coat or matsurface release coat.First discharges coating layer 135 between the lower surface 114 of the upper surface 133 of backing pad 132 and dry-coated material rete 110, preferentially bonds with the upper surface 133 of backing pad 132.Therefore, when release liner 130 by when dry-coated material rete 110 peels off, discharge that coating layer 135 separates with dry-coated material rete 110 and still with backing pad 132 bondings.When laminated material 100 was wound into as shown in Figure 2 roll-good form, the lower surface 137 of releasing layer 136 was adjusted the upper surface 122 that is used for contact adhesive layer 120.
Referring to Fig. 2, dry-coated material transfer laminate 100 is wound into the web-like form, and the lower surface 137 of release coat 136 contacts with the upper surface 122 of adhesive layer 120.Release coat 136 is more solid with the bonding of backing pad 132.Like this, when the dry-coated material transfer laminate 100 shown in Fig. 2 was uncoiled, release coat 136 just separated with adhesive layer 120 and still keeps bond state with backing pad 132.
The dry-coated material transfer laminate 100A shown in Fig. 3 be equal at the dry-coated material transfer laminate 100 shown in Fig. 1, just between dry paint rete 110 and release coating layer 135, inserted transparent film layer 140.Discharge coating layer 135 and on one side, bond with transparent film layer 140, with backing pad 132 bondings, more solid on another side with the bonding of backing pad 132.Like this, when release liner 130 by when transparent film layer 140 peels off, discharge that coating layer 135 separates with transparent film layer 140 and still with keep backing pad 132 bond state.
The dry-coated material transfer laminate 100B shown in Fig. 4 be equal at the dry-coated material transfer laminate 100A shown in Fig. 3, just between dry-coated material rete 110 and transparent film layer 140, placed printed decoration layer 150.
The dry-coated material transfer laminate 100C shown in Fig. 5 be equal at the dry-coated material transfer laminate 100B shown in Fig. 4, just between printed decoration layer 150 and transparent film layer 140, be provided with the second printed decoration layer 160.
The dry-coated material transfer laminate 100D shown in Fig. 6 be equal at the laminated material shown in Fig. 1 100, just do not discharge coating layer 136, and on adhesive layer 120 increase another release liner 170.Release liner 170 comprises: backing pad 172, and it has upper surface 173 and lower surface 174; With release coat 176, cover and stick on the lower surface 174.Release coat 176 is between the upper surface 122 of the lower surface 174 of backing pad 172 and adhesive layer 120, and is and more solid with the bonding of the lower surface 174 of backing pad 172.Like this, when release liner 170 from adhesive layer 120 when being peeled off, release coat 176 separates with adhesive layer 120, and still keeps the bond state with backing pad 172.
Dry-coated material transfer laminate 100E shown in Figure 7 and the laminated material 100 shown in Fig. 1 are equal to, and just laminated material 100E contains the supporting layer 180 between dry-coated rete 110 and adhesive layer 120.
Laminated material 100 is equal to shown in dry-coated material transfer laminate 100F shown in Figure 8 and Fig. 1, and just laminated material 100F contains the separation layer 190 between dry-coated material rete 110 and adhesive layer 120.
Laminated material 100 is equal to shown in dry-coated material transfer laminate 100G shown in Figure 9 and Fig. 1, and just laminated material 100G contains the supporting layer 180 between dry-coated material rete 110 and adhesive layer 120.Laminated material 100G also contains at the dry-coated material rete 110 and the first printed decoration layer 150,160 and 165 that discharges between the coating layer 135.
Dry-coated material transfer laminate 100C is equal to shown in dry-coated material transfer laminate 100H shown in Figure 10 and Fig. 5, just there is not the release liner 130 among the laminated material 100C, and release liner 170 is covered in above the adhesive layer 120, and release coat 176 is between release liner 170 and adhesive layer 120.
The thickness of the dry-coated bed of material or rete 110 can be for about 0.5 to about 1.5 mils (mils), be about 0.5 to about 1.2 mils in one embodiment, are in one embodiment about 0.5 to arrive about 0.9 mil, and are approximately 0.7 mil in one embodiment.The thickness of adhesive layer 120 can change to about 1 mil from about 0.4, and excursion is about 0.4 to about 0.8 mil in one embodiment, and be about 0.4 to arrive about 0.6 mil in one embodiment.The thickness of backing pad 132 can be distributed in from about 0.5 to about 2 mils, is about 0.5 to about 1.5 mils in one embodiment, and be about 0.85 to arrive about 1.05 mils in one embodiment.First thickness that discharges coating layer 135 can change in the scope of about 0.3 mil from about 0.05, be in one embodiment about 0.1 to arrive about 0.2 mil.Second thickness that discharges coating layer 136 can change to about 0.2 mil between about 0.04, be in one embodiment about 0.04 to arrive about 0.15 mil, and is about 0.04 to arrive about 0.08 mil in one embodiment.The thickness of transparent film layer 140 can change to about 0.4 mil from about 0.05, is about 0.05 to about 0.3 mil in one embodiment, and is about 0.2 mil in one embodiment.The thickness of printed decoration layer 150 can change to about 0.15 mil from about 0.02, is about 0.02 to about 0.08 mil in one embodiment.The thickness range of the second printed decoration layer 160 can be from about 0.02 to about 0.15 mil, is about 0.02 to about 0.1 mil in one embodiment.The thickness range of backing pad 172 can be for from about 0.5 to about 2 mils, are about 0.5 to about 1.5 mils in one embodiment, and be about 0.85 to arrive about 1.05 mils in one embodiment.The thickness of release coat 176 can change to about 0.2 mil from about 0.04, is about 0.04 to about 0.15 mil in one embodiment, and be about 0.04 to arrive about 0.08 mil in one embodiment.The thickness that supporting layer 180 can have is for from about 0.3 to about 1.4 mils, be about 0.3 to about 1.1 mils in one embodiment, be in one embodiment about 0.3 to arrive about 0.8 mil, and is about 0.3 to arrive about 0.5 mil in one embodiment.When using supporting layer 180, the gross thickness that dry-coated material rete 110 and supporting layer 180 combine can from about 0.5 in the scope of about 1.5 mils, be about 0.5 to about 1.2 mils in one embodiment, be about 0.5 to about 0.9 mil in one embodiment, and be about 0.7 mil in one embodiment.The thickness of separation layer 190 can have at about 0.01 thickness within about 0.1 mil scope, be about 0.05 to about 0.1 mil in one embodiment, and is about 0.01 to arrive about 0.02 mil in one embodiment.In above-mentioned each thickness each all is dry thicknesses of layers.Laminated material 100 has any width and length up to 100H, and it is suitable for the convenient of user and uses.For example, width can change to about 200cm from about 1, is 10 to 100cm in one embodiment, and be in one embodiment about 30 arrive about 40cm (centimetre).The excursion of length is from about 10 to about 6500m, is about 15 to about 1000m (rice) in one embodiment.In one embodiment, length can change the scope from about 19 to about 6500m.In one embodiment, length can change in about 20 meters scope about 17.In one embodiment, the width that laminated material can have is about 10 to about 20cm, and length is about 10 to about 30cm.Laminated material can be provided in the mode that is dull and stereotyped form, or the web-like form that is as shown in Figure 2 is provided.
Layer 110,150,160 and 165 can comprise one or more base-materials (binding agent (binders)) or resin independently of one another, and one or more pigment.Supporting layer 180 can comprise one or more binding agents or resin, and randomly, comprises one or more pigment.Transparent film layer 140 can comprise one or more binding agents or resin.These layers can make with liquid coating or paint composite, liquid coating or paint composite comprise these one or more binding agents or resin, these one or more pigment (if you are using), water or one or more organic solvents, and randomly, comprise one or more additional additives in order to control character such as rheological property and similarity.Layer 110,140 and 180 all comprises one or more layers extruded polymer film independently of one another.
Binding agent (binder) or resin (resin) can comprise any binding agent or the resin that uses traditionally in coating or paint formulation.Binding agent (binder) can comprise thermoplasticity or thermosetting resin.Binding agent or resin can be synthetic resin or natural resin.Binding agent or resin can comprise filmogen, and in one embodiment, it can be squeezable film forming matter.The useful binding agent or the example of resin comprise acrylic resin, vinyl, mylar, alkyd resins, poly-fourth resin, styrene resin, phthalic resin or phthalic anhydride resin, polyurethane resin, epoxy resin and analog.Binding agent or resin can comprise vinyl and ethenylidene polymer or copolymer, and it comprises as vinyl acetate, vinyl chloride, the inferior ethene of chlorine and similar monomer; Hydrocarbon polymer and copolymer, it comprises ethene or propylene monomer; And the oxidation or the halide derivative of ether, butadiene, oxidation butadiene, isoprene, oxidation isoprene, butadiene-styrene, butadiene ethylbenzene, isoprene-styrene etc.; Comprise acrylic acid, methacrylic, their ester class or the polymer or the copolymer of acrylonitrile monemer; The vinyl hydro carbons monomer that reacts with unsaturated materials such as maleic acid or maleic anhydride and cinnamic product; And in a general sense, other are various to have the resin type rubber-like elasticity emulsion polymer and the copolymer of unsaturated vinyl monomer and the available polymer that is hydration latex form stable existence.Binding agent or resin can comprise the copolymer of vinyl chloride and vinyl acetate.Binding agent or resin can comprise '-diphenylmethane diisocyanate, methylene diethyl vulcabond, isocyanuric acid ester, ureaformaldehyde, phenol formaldehyde (PF), phenol glue, animal skin glue, or the like.The binding agent that other may adopt or the example of resin comprise fluororesin, organic siliconresin (silicone resins) and fibre resin (fibrin resins).
Binding agent or resin can comprise one or more polystyrene, polyolefin, polyamide, polyester, Merlon, polyvinyl alcohol, polythene-ethenol, polyurethane, polyacrylate, polyvinyl acetate, ionomer and composition thereof.Polyolefinic feature can be its melt flow index or melt flow rate (MFR) less than about 30, in one embodiment less than about 20 with in one embodiment less than about 10, as what measured with ASTM method of testing 1238.
Polyolefin comprises the polymer and the copolymer of ethene, propylene, butene-1 etc., or the blend of the mixture of these polymer and copolymer.Polyolefin can comprise the polymer and the copolymer of ethene and propylene.Polyolefin can comprise Noblen and copolymer such as propylene-ethylene and propylene-butene-1 copolymer.Can use polypropylene and polyethylene blend each other, perhaps, the two one or both of with the blend of polypropylene-polyethylene and ethylene copolymers.The polyolefin film forming matter can have high propylene content, or the propylene-ethylene copolymers of polypropylene homopolymer or low ethylene content or polypropylene and poly blend, or the blend of the propylene-butene-1 copolymer of low butene content or polypropylene and PB Polybutene-1.
Can use various polyethylene, comprise basic, normal, high density polyethylene.For polyethylene kind, the low-density scope can be to about 0.925g/cm from about 0.910
3, middle density range can be to about 0.940g/cm from about 0.925
3, the high density scope can be to 0.965g/cm from about 0.940
3A kind of example of useful low density polyethylene (LDPE) (LDPE) is the Rexene 1017 that can derive from Huntsman company.
Can use separately or with the Noblen that propylene copolymer is used in combination, comprise diversified Noblen, for example have those of melt flow (MFR) from about 0.5 to about 20, be that condition L measures with ASTM Test D 1238 methods.In one embodiment, the MFR value of operable Noblen is less than about 10, and is from about 4 to about 10 in one embodiment.The feature of Noblen can be to have density range about 0.88 to 0.92g/cm
3Many available Noblens all have various commercial source, some available polymer comprise: 5A97, can derive from Union Carbide company, and the melt flow that has is 12.0g/10min, density is 0.90g/cm
3DX5E66 also can derive from Union Carbide company, and its MFI value is 8.8g/10min, and density is 0.90g/cm
3And from the WRD5-1057 of UnionCarbide company, its MFI value is 3.9g/10min, and density is 0.90g/cm
3The Noblen of available commercial source also can obtain from Fina and Montl company.
Polyamide comprises can be from EMS American Grilon company, the resin that Sumter, SC obtain, and its general trade mark is Grivory, for example CF6S, CR-9, XE3303 and G-21.Grivory G-21 is a kind of amorphous nylon copolymer, and its glass transition temperature is 125 ℃, and melt flow index (DIN53735) is 90ml/10min, and extension at break (ASTM D638) is 15.Grivory CF65 is nylon 6/12 film grade resins, and its fusing point is 135 ℃, and melt flow index is 50ml/10min, and extension at break surpasses 350%.Grilon CR9 is another kind of nylon 6/12 film grade resins, and its fusing point is 200 ℃, and melt flow index is 200ml/10min, and extension at break is 250%.Grilon XE3303 is a kind of nylon 6.6/6.10 film grade resins, and its fusing point is 200 ℃, and melt flow index is 60ml/10min, and extension at break is 100%.Polyamide comprises the resin in following source, for example, under the Uni-Rez product line, from the product of the Union Camp company in the Wayne city that is positioned at the New Jersey, and can be from Bostik, Emery, Fuller, the dimer based polyamide resin of Henkel (under the Versamid product line).Polyamide comprises that those are via dimerized vegetable acids and hexamethylene diamine condensation and the product that obtains.The example that can derive from the polyamide of Union Camp company comprises Uni-Rez 2665, Uni-Rez 2620, Uni-Rez 2623; With Uni-Rez 2695.
Polystyrene comprises the homopolymers and the copolymer of styrene and substituted phenylethylene such as AMS.The example of styrol copolymer and terpolymer comprises: acrylic nitrile-butadiene-alkene-styrene (ABS); SAN (SAN); Styrene-butadiene (SB); Phenylethylene-maleic anhydride (SMA); And styrene-methyl methacrylate (SMMA); Or the like.
Polyurethane comprises aliphatic and aromatic urethane.
Polyester can make from various ethylene glycol or polyol and one or more aliphatic or aromatic carboxylic acid.PET (PET) and PETG (with the PET of cyclohexanedimethanol modification) are available filmogens, can obtain from multiple commercial source, comprise Eastman company.For example, Kodar6763 is a kind of PETG product that can obtain from Eastman Chemical company.Another kind of available polyester is that E.I.Du Pont Company's trade mark is the PET of Selar PT-8307.
Can adopt acrylic polymer and copolymer and alkylidene vinyl acetate resin (as the EVA polymer).Example comprises Escorene UL-7520 (Exxon), a kind of ethylene copolymer that contains 19.3% vinylacetate; Nucrell 699 (Du Pont (DuPont)), a kind of ethylene copolymer that contains 11% methacrylic acid, etc.
Can adopt ionomer (polyolefin that contains the strand ionic bond).Its example comprises the ethylene copolymer that contains iolon, as Surlyn 1706 (Du Pont), it is said that it is the interchain ionic bond that contains based on the zinc salt of ethylene-methacrylic acid copolymer.Surlyn 1702 from E.I.Du Pont Company is a kind of spendable iolons.
Merlon also is useful, and these can obtain from Dow chemical company (Calibre), G.E.Plastics (Lexan) and Bayer company (Makrolon).This Merlon is can carry out interfacial reaction by bisphenol-A and phosgene to obtain.Molecular weight can change from about 22000 to about 35000, and melt flow can be in about scope of 4 to about 22g/10min.
Pigment (pigment) can be for making any pigment that uses in the decorative coveringn.They comprise opaque pigment such as titanium dioxide and zinc oxide, and coloring pigment such as carbon black, oxide yellow thing, brown oxide, sepia oxide, nature and the loess of firing or umber, chrome oxide green, phthalocyanine green, phthalocyanine blue, celestine blue, cadmium pigment, chromium pigment and analog.Pigment comprise organic red as azophloxine, quinoline a word used for translation ketone is red and perylene is red, and organic yellow such as diarylide yellow.Can adopt mixed-metal oxides pigment.Can add extender pigment such as clay, silica (silica), talcum powder, mica, wollastonite wood powder, barium sulfate, calcium carbonate, alumina silicate and analog, its addition is identical with employed traditional content in coating and paint formulation.
Solvent (solvent) can be based on organic solvent, as ketone, ether, aliphatic compound, aromatic compound, alcohol, ethylene glycol, glycol ether etc.They comprise butanone, methyl iso-butyl ketone (MIBK), ethyl acetate, petroleum solvent, alkane, cycloalkane, benzene, replacement hydrocarbon aromatic (as toluene, xylene, or the like), isoparaffin solvent and two or more mixture wherein.Alternatively, can make water or group water solution, form emulsion with binding agent or resin.Group water solution comprises water-crude alcohol mixture and similar substance.Solvent or water have enough volatility, when making that be used in ground (substrate) goes up, and solvent evaporation and stay the involatile constituent of binding agent or resin, pigment (if you are using) and any other interpolation.
The adding ingredient of using comprises wetting agent, plasticizer, suspension aids, thixotropic agent such as silica, waterproof additive such as polysiloxane compound, flame-retardant additive, biocide, defoamer, flowable and analog.
Be used for providing the liquid paint of layer 110,150,160 and 165 or coating composition pigment concentration can by weight, change in about 30% scope from about 10, be about 13 to about 27% in one embodiment by weight.The concentration of binding agent or resin can change in about scope of 20 to about 40wt.%, is about 22 to about 37wt.% in one embodiment.The excursion of water or organic solvent concentration can be from about 30 to about 70wt.%, is about 40 to about 60wt.% in one embodiment.Adding ingredient such as wetting agent, suspending agent can be provided with concentration known in the art, for example up to about 5wt.%, are about 0.1 to about 5wt.% in one embodiment.The pigment volume concentration (PVC) (pigment volume concentration (PVC)) that used coating or paint composite can contain in prepared layer 110,150,160 and 165 is from about 5 to about 35% scope, is 10 to about 30% in one embodiment.Can adopt known technology to mix to being used for prepared layer 110,150,160,165 and 180 applied liquid coatings or paint composite.
The dry-coated bed of material or rete 110 can comprise signal layer coating or the laminated coating that is made of paint, be the form of pantostrat, and printed decoration layer 150,160 and 165 can be the form of pantostrat or discontinuity layer separately independently.When layer 110 adopted laminated coating, each coating can have same recipe or different prescriptions.Layer 150,160 and/or 165 with layers 110 color can be identical or different.The color of layer 150,160 and/or 165 can be identical, or they have mutually different color.Layer 110 can be used as background color is provided, and layer 150,160 and/or 165 can be used as style or pattern are provided.For example, layer 150,160 and/or 165 can be manual simulation's facing or " embossing " shape or " sponge " shape.Layer 150,160 and/or 165 can be used, and is used to provide the printed article with one or more colors or the design (as the design of style) of expectation.Design can be the repeat patterns or the form of not repeat patterns at random.
Hyaline layer or rete 140 can comprise signal layer coating or multilayer coated layer, can comprise above-mentioned any resin material.When using multilayer coated layer, every layer formula can be identical or different.But transparent film layer 140 extrusion moldings.The object lesson of the resin that can be used comprises: the copolymer of polyvinyl chloride and vinyl chloride and acrylic or methacrylic acid.Transparent film layer 140 is that it is the transparent or semitransparent fact with the main distinction of dry paint rete 110.In one embodiment, transparent film layer 140 can strengthen mar proof, stain resistance and/or the recoatability of dry paint rete or following lining layer in its lower section.The recoatability that strengthens is meant following character, and promptly having of transparent film layer 140 helps add afterwards one deck dried film or printed decoration layer on it, perhaps uses traditional coating or body of wall covering (as wallpaper) on it again.
Supporting layer 180 can be made with above-mentioned any binding agent or resin material.Supporting layer can make with solution or emulsion, adopts following any coating technology coating.But supporting layer 180 extrusion moldings.Supporting layer 180 can comprise one or more above mentioned pigment.In one embodiment, supporting layer 180 comprises enough pigment, and even provides muted color such as grey, light blue, pale red etc. to it.When being used, the variation of the concentration range of pigment can be about 6 to about 10wt.% (percentage by weight) up to about 10wt.% in one embodiment in the supporting layer 180.
Layer 110,140 and 180 can comprise inorganic filler or other organic or inorganic additive independently of one another, to produce the character of expectation, as appearance characteristics (clear, opaque or Coloured film), durability and operational characteristic.Available example of material comprises calcium carbonate, titanium dioxide, metallic particles, fiber, fire retardant, anti-oxidant compounds, heat stabilizer, light stabilizer, UV light stabilizing agent, anticaking agent, processing aid, acid acceptor etc.
Add nucleator (nucleatingagents) in one or more layers that can be in layer 110,140 or 180, improving degree of crystallinity, thereby improve hardness.Can use the nucleator of usefulness to comprise inorganic nucleator and organic nucleating agent.The example of inorganic nucleator comprises carbon black, silica, kaolin and mica.The example of organic nucleating agent comprises the salt of fatty monobasic or binary acid or aryl acid, for example sodium succinate, Sodium glutarate, sodium n-caproate, 4-methylvaleric acid sodium, phenylacetic acid aluminium and sodium cinnamate.The alkali metal salt of aromatic series and alicyclic carboxylic acid and aluminium salt such as benzoic acid aluminium, sodium benzoate or potassium, β sodium phenate, benzoic acid lithium and tert-butyl group benzoic acid aluminium also are available organic nucleating agents.Wherein alkyl contains that to have an appointment 2 also be available nucleator to the replacement sorbitol derivatives of about 18 carbon atoms such as two (benzals) and two (alkyl benzal) D-sorbites.Also can use as 1,3,2,4-dibenzylidene sorbitol, 1,3,2,4-are to dimethyl benzylidene D-sorbite and 1,3,2, and 4-is to the sorbitol derivatives of dimethyl benzylidene D-sorbite.Become the addition excursion of nucleator in the film formulation can be about 100 to about 6000ppm of film.In one embodiment, the amount of nucleator can be about 1000 to about 5000ppm.
One or more layers can comprise a small amount of tackifying resin in the layer 110,140 or 180, arrives the bonding of layer 140 and/or 180 with enhancement layer 110.And perhaps alternatively, the tack coat of tackifying resin can be between layer 110 and 140 or between the layer 110 and 180.Tackifying resin can be the copolymer of Ethylene/vinyl acetate, is the product of Elvax as the trade mark of E.I.Du Pont Company (DuPont).Also can use the trade mark that can derive from E.I.Du Pont Company tackifying resin as Bynel.
In one embodiment, the layer 110,140 and/or 180 at room temperature for do not extend with stiff.
Adhesive layer 120 can comprise that pressure-sensitive adhesive (pressure sensitive adhesive (PSA)) layer, moisture activate adhesive layer or hot activation adhesive layer.Adhesive can comprise known in the art be used for the film ground any pressure-sensitive, moisture is that activate and heat activated adhesive.Adhesive layer 120 can be continuous or discrete form, can comprise the mixture of a kind of adhesive or two or more adhesives.Adhesive layer can be the adhesive layer of pattern form, and some regional viscosity are stronger, other regional viscosity a little less than.In one embodiment, adhesive layer provides initial viscosity, and the tolerable laminated material slightly moves, so that adjust the position before forming secure bond.In one embodiment, when no longer the coating rete was used in expectation, adhesive therefor helped to peel off the dry paint rete from ground.In one embodiment, the feature of adhesive layer is when implementing laminated material on ground, only produces limited amount leakage outside the border of laminated material.In one embodiment, then do not leak.Adhesive comprises rubber-based adhesive, acryloid cement, vinyl ethers adhesive, silicone adhesive or two or more mixture wherein.During use, adhesive can be heat molten type, solvent-borne type or water-based adhesive.As main component, available adhesive can comprise sticky polymers as main constituent, as acrylic polymer; Block copolymer; Natural rubber, reclaimed rubber or SBR styrene butadiene rubbers; Natural or the synthetic rubber that viscosity strengthens; The copolymer of ethene and vinylacetate; Vinyl-vinyl-acrylic acid terpolymer; Polyisobutene; Poly-(vinethene) etc.Other material such as viscosity that can be included in the adhesive strengthens resin, plasticizer, antioxidant, filler, paraffin etc.
Adhesive can be divided into following classification: the random copolymer adhesive, as based on the copolymer of acrylate and/or methacrylate, alpha olefin copolymer, silicone copolymer, chlorobutadiene/acrylonitrile copolymer etc.; Block copolymer adhesive comprises line-type block polymer (being A-B and A-B-A type), branched block copolymer, star block copolymer, grafting or radial block copolymer etc.; And natural and synthetic rubber binder.Description to available formation of pressure-sensitive adhesive layer is found in Encyclopedia of Polymer Science and Engineering, Vol.13.Wiley-Interscience Publishers (New York, 1988).The other description of available formation of pressure-sensitive adhesive layer is found in Encyclopedia of Polymer Science and Technology, Vol.1.Interscience Publishers (New York, 1964).
Available formation of pressure-sensitive adhesive layer comprises the heat fusing formation of pressure-sensitive adhesive layer, can obtain the trade mark such as HM-1597, HL-2207-X, HL-2115-X, HL-2193-X from the H.B.Fuller company that is positioned at Minnesota State St.Paul.Other available formation of pressure-sensitive adhesive layer comprises the product that can derive from the Century Adhesive company that is positioned at Ohio Columbus.
Also traditional PSA be can use, silicone base PSA, rubber-based PSA and acrylic PSA comprised.The example of another commercial source of hot melt adhesive is the H2187-01 that is sold by the Ato Findley company that is positioned at state of Wisconsin Wauwatusa.Remove this, also can use patent US3, the described rubber-based block copolymer of 239,478 (Harlan), the disclosure that is incorporated herein hot melt adhesive in this patent is as a reference.
In one embodiment, formation of pressure-sensitive adhesive layer comprises the rubber-based elastomeric material, for example line style, side chain, grafting or radial block copolymer, be expressed as diblock structure A-B, three block A-B-A, radially or coupling structure (A-B) n, and their combination, wherein A represents that hard thermoplasticity mutually or block, it at room temperature is nonrubber shape or glassy or lenticular, but at high temperature be fluid, B represents soft block, and it in use or be rubber-like or flexible under the room temperature.These thermoplastic elastomer (TPE)s can comprise that about 75wt.% arrives the rubber-like segment of about 95wt.% and the nonrubber shape segment that about 5wt.% arrives about 25wt.%.
Nonrubber shape segment or hard block comprise the polymer of monocycle or polycyclic aromatic hydrocarbon, more specifically, promptly are essentially the vinyl substituted arene of monocycle or dicyclo.Rubber-like block or segment are typically the polymer blocks of aliphatic conjugated diene homopolymers or copolymer.Can use elastomeric material such as polyisoprene, polybutadiene and butadiene-styrene rubber to form rubber-like block or segment.The rubber-like segment comprises the polydiene and the saturation of olefins rubber of ethylene/butylene or ethylene/propene copolymer.The latter can be obtained by hydrogenation reaction by corresponding unsaturated polyester alkylene moiety such as polybutadiene and polyisoprene.
The block copolymer of available vinyl-arene and conjugated diene comprises any copolymer with elastomeric properties.This block copolymer can be diblock, three blocks, many blocks, star block, poly-block or graft block copolymer.In this specification and claims, about the standard implication of the term diblock of block copolymer structure feature, three blocks, many blocks, star block, poly-block and grafting block is defined their common connotation in the document, for example following document defines: Encyclopedia of Polymer Science and Engineering, Vol.2, John Wiley ﹠amp; Sons (1985), New York, pp.325-326 and author are the Block Copolymers of J.E.McGrath, Science Technology, and Dale J.Meier, Ed., 1979, Harwood Academic Publishers is in the 1-5 page or leaf.
The conjugated diene that this block copolymer contains and the ratio of vinyl-arene can be various, comprise the vinyl-arene that contains up to about 40%, calculate by weight.Therefore, can use line style or radial symmetric or asymmetric segmented copolymer, its structure can be used general formula A-B, A-B-A, A-B-A-B, B-A-B, (AB) 0,1, expressions such as 2...BA, wherein A is the polymer blocks of vinyl-arene or the alternation copolymer block of conjugated diene/vinyl arene, and B is the rubber-like polymer block of conjugated diene.
Available any well-known block polymerization of the preparation of block copolymer or copolymerization process comprise that continuous adding monomer, increment add monomer or coupling technology, for example as patent US3,251,905; 3,390,207; 3,598,887 and 4,219,627 set forth like that.As everyone knows, utilize different copolyreaction speed, the alternation copolymer block can embed segmented copolymer by the mixture of copolymerization conjugated diene and vinyl aromatic monomer.Many patents are described the preparation of the segmented copolymer that comprises the alternation copolymer block, comprise patent US3,251,905; 3,639,521 and 4,208,356, be incorporated herein its disclosure as a reference.
The conjugated diene that is used to prepare polymer and copolymer contains 4 to about 10 carbon atoms, more is commonly 4 to 6 carbon atoms.Example comprises 1,3-butadiene, 2-methyl isophthalic acid, 3-butadiene (isoprene), 2,3-dimethyl-1,3-butadiene, chlorobutadiene, 1,3-pentadiene, 1,3-hexadiene etc.Also can use the mixture of these conjugated dienes.Preferred conjugated diene is isoprene and 1,3-butadiene.
The example that is used to prepare the vinyl-arene of copolymer comprise styrene and various substituted phenylethylene such as neighbour-methyl styrene, p-methylstyrene, right-t-butyl styrene, 1,3-dimethyl styrene, AMS, Beta-methyl styrene, right-cumene ethene, 2,3-dimethyl styrene, neighbour-chlorostyrene, right-chlorostyrene, neighbour-bromstyrol, 2-chloro-4-methyl styrene etc.Preferred vinyl-arene is a styrene.
In the copolymer of above-mentioned conjugated diene and vinyl-arene, many can both having bought.Before the hydrogenation, the mean molecule quantity of block copolymer is about 20000 to about 500000, is preferably about 40000 to about 300000.
The mean molecule quantity of single block changes in a certain boundary in the copolymer.In most cases, the mean molecule quantity of vinyl-arene block is about 2000 to about 125000, is preferably about 4000 to 60000.Before and after the hydrogenation, the mean molecule quantity of conjugated diene block is about 10000 to about 450000, more preferably about 35000 to 150000.
Before the hydrogenation, the ethylene contents of conjugated diene part is about 10% to about 80%, is preferably about 25% to about 65%, is specially 35% to 55% when the block copolymer of expectation modification has caoutchouc elasticity.The ethylene contents of block copolymer can be used nmr for the determination.
The object lesson of diblock copolymer comprises styrene-butadiene (SB), styrene-isoprene (SI) and hydroderivating thing thereof.The example of triblock polymer comprises s-B-S (SBS), styrene-isoprene-phenylethene (SIS), AMS-butadiene-AMS and AMS-isoprene-AMS.The commercial available block copolymer that can be used as adhesive of the present invention comprises the product of Shell Co. Ltd, lists in following Table II.
Table II
Kraton | Type | Styrene/rubber is than (w) | Melt index |
D1101 D1107P D1111 D1112P D1113P | Type SBS line style SIS line style SIS line style SIS line style SIS | 31/69 15/85 22/78 15/85 16/84 | <1 11 3 23 24 |
D1117P D1320X | Line style SIS racemosus (Multi-arm) is n (SI) | 17/83 10/90 | 33 NA |
Vector 4111 SIS block copolymer for buying from the Dexco company of Texas state Houston.
By SBS copolymer hydrogenating, obtain styrene-ethylene-butylbenzene ethene (SEBS) block copolymer to the rubber-like segment that comprises 1,4 and 1,2 isomer mixture.Equally, the SIS hydrogenation of polymer obtains styrene-second propylene-styrene (SEPS) block copolymer.
The selective hydrogenation of block copolymer can realize with various well-known methods, is included under the existence of catalyst such as Raney nickel, noble metal such as platinum, palladium etc. and solvable transition-metal catalyst to carry out hydrogenation.Adoptable suitable method of hydrotreating is that polymer or the copolymer that will contain diene are dissolved in inertia hydrocarbon diluent such as the cyclohexane, and carries out the method for hydrogenation in the presence of solvable hydrogenation catalyst with H-H reaction.These methods are at patent US3, description are arranged in 113,986 and 4,226,952, are incorporated herein its disclosure as a reference.The hydrogenation of block copolymer proceeds to a certain degree in a certain way, produces the selective hydrogenation copolymer, and the unsaturated amount of residue is about 0.5% to about 20% of the preceding initial unsaturated amount of hydrogenation in the polydiene block.
In one embodiment, the conjugated diene of block copolymer part at least 90% is by saturated, and more frequent is at least 95% by saturated, and vinyl-arene is not partly obviously by hydrogenation.Available hydrogenation block copolymer comprises the SIS hydrogenation products, as styrene-(ethylene/propene)-styrenic block polymers.When polystyrene-poly butadiene-polystyrene block copolymer hydrogenation, in the expectation polymer 1,2-polybutadiene and 1, the ratio of 4-polybutadiene is about 30: 70 to about 70: 30.What the product type that such block copolymer hydrogenation forms was similar to ethene and 1-butylene (EB) has a rule copolymer block.When conjugated diene was isoprene, what the hydrogenation products of generation was similar to ethene and propylene (EP) had a rule copolymer block.
Commercial, there is the block copolymer of many selective hydrogenations in Shell Co. Ltd, and its general trade mark is " Kraton G ".An example is Kraton G1652, and it is the SBS triblock polymer of hydrogenation, comprises the mid-block of about 30wt.% styrene end block and ethene and 1-butylene (EB) copolymer.The G1652 than small-molecular weight of Shell Co. Ltd is Kraton G1650.KratonG1651 is that another kind comprises the cinnamic SEBS block copolymer of about 33wt.%.KratonG1657 is for containing the cinnamic SEBS diblock copolymer of the 13wt.% that has an appointment.Its styrene-content is lower than styrene-content among Kraton G1650 and the Kraton G1652.
In another embodiment, the selective hydrogenation block copolymer has general formula
B
n(AB)
oA
p
Wherein: n=0 or 1; O=1-100; P=0 or 1; Before the hydrogenation, B mainly is the conjugated diene block of polymerization, and its mean molecule quantity is about 20000 to about 450000; A mainly is the vinyl-arene block of polymerization, and its mean molecule quantity is about 2000 to about 115000; Block A contains the copolymer of 5wt.% to about 95wt.% of having an appointment; The degree of unsaturation of B block is less than about 10% of initial degree of unsaturation.In one embodiment, the degree of unsaturation of B block is reduced to behind hydrogenation less than 5% of initial value, and the average degree of unsaturation of hydrogenation block copolymer is reduced to less than 20% of initial value.
Block copolymer also comprises functionalized polymer, for example by adding α, β-alkene unsaturated monocarboxylic acid or dicarboxylic acids reagent reacts the product that obtains on the selective hydrogenation block copolymer of above-mentioned vinyl-arene and conjugated diene.React between carboxylic acid in this graft block copolymer and can in solution or in the melting process that radical initiator exists, realize.
The various selective hydrogenation block copolymers of conjugated diene and vinyl-arene have description with the preparation method of carboxylic acid reagent grafting in many patents, comprise US 4,578,429; US 4,657, and 970 and US 4,795,782, be incorporated herein in these patents the disclosure relevant as a reference with the preparation of the selective hydrogenation block copolymer of the conjugated diene of grafting and vinyl-arene and these compounds.Patent US 4,795, and 782 describe and provide the solution of graft block copolymer and the preparation embodiment of melting method.Patent US 4,578, and an embodiment is on double screw extruder in 429, by frit reaction, with containing 2,5-dimethyl-2, maleic anhydride graft Kraton G1652 (SEBS) polymer of 5-two (tert-butyl peroxy) hexane.
Commercial, the maleic acid selective hydrogenation copolymer of styrene and butadiene comprises Kraton FG1901X, FG1921X and the FG1924X of Shell Co. Ltd, is often being claimed maleic acid selective hydrogenation SEBS copolymer.FG1901X comprises succinic anhydride and the about 28wt.% styrene that about 1.7wt.% signs an undertaking and closes function.FG1921X comprises succinic anhydride and the about 29wt.% styrene that about 1wt.% signs an undertaking and closes function.FG1924X comprises about 13wt.% styrene and about 1wt.% and signs an undertaking and close the succinic anhydride of function.
Available block copolymer also can be from being positioned at Tokyo Chiyoda-ku, Marunochi, and the Nippon Zeon company of 2-1 obtains.For example, from the available Quintac3530 of Nippon Zeon company, a kind of line style SIS.
Adhesive composition can comprise at least a solid tackifer resin composition.Here, the solid tackifier are defined as its softening point more than 80 ℃.When containing solid tackifer resin, adhesive composition comprises about 40 to about 80wt.% thermoplastic elastomer component and about 20wt.% to about 60wt.%, about 55 arrives about 65wt.% solid tackifer resin composition in one embodiment.The solid tackifier reduce the mixture modulus, make it have enough viscosity or adhesive force.The solid tackifier of solid tackifier (particularly have HMW (as Mw greater than about 2000) and low diffusance (Mw/Mn≤about 3)) be difficult for moving to polymer film, this expects, can cause its shape instability because tackifier enter rete 110 or 180.
Solid tackifer resin comprises that hydrocarbon resins, rosin, hydrogenation rosin, rosin fat, polyterpene resin and other have the resin of appropriate balance character.Commercial have various available solid tackifer resins, a for example Zonatac board terpene resin of Arizona chemical company, and the Escorez board resin of petroleum hydrocarbon resin such as Exxon company.An object lesson of available solid tackifier is Escorez 2596, and it is C
5-C
9(aromatic modified aliphatic) synthesizes tackifier, and Mw is 2100, and diffusance (Mw/Mn) is 2.69.Another kind of available solid tackifier are Escorez1310LC, and it is an aliphatic hydrocarbon resin, and Mw is 1350, and diffusance is 1.8.Wingtack 95 is Ohio state Akron, and the synthetic tackifier of Goodyear company mainly are made up of the paradigmatic structure of piperylene and isoprene.
By adding at room temperature is the liquid rubber of liquid, can reduce the modulus of the binder combination of extruding simultaneously.The molecular weight of liquid rubber is at least 5000 usually, is more typically at least 20000.Adding is less than the 10wt.% of adhesive gross weight, even makes adhesive together to push with the polymeric membrane material less than 5% liquid rubber.The adding of liquid rubber can improve the viscosity and the adhesive force of adhesive.Also can adopt liquid block copolymer such as liquid styrene-isoprene block copolymer.Example comprises the Kraton LVSI-101 of Shell Co. Ltd.Another example is the liquid polyisoprene that the HMW polyisoprene obtains after depolymerization.A commercial example of the HMW polyisoprene of depolymerization is N.J., the Isolene D-400 of the Elementis PerformancePolymers company of Belleville, the molecular weight of this liquid rubber about 20000.Other liquid rubber that can add binder combination comprises liquid SBR styrene butadiene rubbers, liquid butadiene rubber, ethylene-propylene rubber etc.
Adhesive compound also can comprise other materials such as antioxidant, heat and light stabilizer, UV absorbers, filler, colouring agent, anticaking agent, reinforcing agent, processing aid etc.Hindered phenolic and amine antioxidant compound can be included in the adhesive composition, and multiple this type of antioxidant compound is known in the art.Can obtain various antioxidant from Ciba-Geigy company, its trade mark is " Irganox " and " Irgafos ".For example, the trade mark of hindered phenolic antioxidant n-octadecane base-3-(3,5-di-t-butyl-4-resorcinol)-propionic ester (proprionate) is " Irganox1076 ".Irganox 1010 be accredited as four (methylene 3-(3 ', 5 '-di-t-butyl-4 '-resorcinol) propionic ester (proprionate)) methane.Irgafos 168 is the antioxidant of the available Ciba-Geigy company of another kind.Also can use hydroquinones base antioxidant, one of them example is 2,5-two tertiary pentyl hydroquinones.Also can comprise light stabilizer, heat stabilizer and UV absorbers in the adhesive compound.UV absorbers comprises benzotriazole derivatives, hydroxyl benzyl benzene ketone (hydroxy benzyl phenones), benzoic ether, oxalic acid, hydrazine etc.Light stabilizer comprises interrupted amine light stabilizer, and heat stabilizer comprises dithiocar-bamate component such as zinc dibutyl dithiocarbamate.
Adhesive compound can comprise inorganic filler and other can provide the organic and inorganic additive of desirable properties.Available filler example comprises calcium carbonate, titanium dioxide, metallic particles, fiber etc.Available end block reinforcing agent example is the Cumar LX509 of Neville Resins company.
Percentage by weight
Separation layer No.1
Elvacite 2042 (product of Ineos, 20
A kind of ethyl-methyl acrylate copolymer)
Toluene 48
MEK 32
Separation layer No.2
Adcote 61 WG178(Rohm and 0.10
The product of Haas, acrylic acid polymer solution)
Syloid 234 (product of Grace Davidson,
Synthetic amorphous silica gel)
Normal propyl alcohol 44.35
Separation layer No.3
Adcote 61 WG178 74.07
Normal propyl alcohol 25.83
Syloid 234 0.10
Separation layer No.4
Adcote 61 WG178 55.55
Normal propyl alcohol 44.35
Syloid 234 0.10
Desmodur CB 75N (Bayer product, 0.44
Oligomeric toluene di-isocyanate(TDI))
Separation layer No.5
Adcote 61 WG178 74.07
Normal propyl alcohol 25.83
Syloid 234 0.10
Desmodur CB 75N 0.44
Separation layer No.6
Adcote 61 WG178 58.0
R-900TiO
2(DuPont product, 15.00
Rutile titanium dioxide)
Normal propyl alcohol 24.0
Isobutanol 3.00
Separation layer No.7
Adcote 61 WG178 58.00
R-900TiO
2 15.00
Normal propyl alcohol 24.00
Isobutanol 3.00
Desmodur CB 75N 0.88
Separation layer No.8
Air Vol 523 (Air Products product, 5.0
Polyvinyl alcohol)
Water 47.5
Isopropyl alcohol 47.5
Alternatively, backing pad 132 and 172 can comprise polymer film independently of one another, and its example comprises polyolefin, polyester and its combination.Polyolefin film comprises and contains 2 polymer and copolymers to the monoolefine of about 12 carbon atoms, is 2 to about 8 carbon atoms in one embodiment, and per molecule is 2 to about 4 carbon atoms in one embodiment.The example of this homopolymers comprises polyethylene, polypropylene, poly-1-butylene etc.The film that can adopt the mixture by the mixture of copolymer or copolymer and homopolymers to make.These films can be extruded into single or multiple lift.
The another kind of material that can be used as backing pad 132 and 172 is the kraft liner of overbrushing layer, and it is made up of the ox-hide paper washer that one or both sides all scribble polymer coating substantially.By high, in or the polymer coating formed of low density polyethylene (LDPE), propylene, polyester or other similar polymer film be coated in surface of bottom material, the intensity and/or the shape stability of increase liner.The weight of this pad is about 30 to about 100 pounds/order, and used weight is about 94 to about 100 pounds/order.Generally speaking, final backing pad 132 comprises about 10% to about 40% polymer and about 60% to about 90% paper.When all there is coating on the two sides, the roughly uniform distribution of amount of polymers of above the paper and paper bottom surface.
In one embodiment, backing pad 132 and 172 gives laminates structural integrity, has been used on the ground up to laminated material just to be removed.Since use these two liners or one of, just not be used in and use semirigid in the laminated material of the present invention or strengthen the plate that supports.
Discharge coating layer 135 and comprise single or multiple lift release coat material.When adopting laminated coating, every layer formula can be identical, also can use different prescriptions.Discharge coating layer 135 and can comprise above-mentioned any binding agent or resin, make to discharge between coating layer 135 and dry paint rete 110 (Fig. 1 or 6-8), transparent film layer 140 (Fig. 3-5) or the printed decoration layer 165 (Fig. 9) and have enough viscosity or adhesive force, thereby stop discharging coating layer 135 separates with rete 110,140 or 165 during the dry-coated material transfer laminate of preparation and normal running laminated material, also make it have enough fissilities, to promote that discharging coating layer 135 separates with layer 110,140 or 165 when using laminated material.Discharging coating layer 135 can comprise and staggered alkyd resins and/or the vinyl that links to each other of melamine resin.Alkyd resins comprises one or more polyalcohols and one or more polyacids or acid anhydrides condensation and the resin that forms.Polyalcohol comprises glycerine, and polyacid or acid anhydrides comprise phthalic anhydride.Can adopt the alkyd resins of modification, wherein polyacid is by monoacid such as acrylic acid or the replacement of vegetable fatty acid moieties.Available vinyl comprises copolymer, acrylic resin, methacrylic resin, polystyrene resin of polyvinyl chloride, polyvinyl acetate, vinyl chloride and vinylacetate etc.Melamine resin comprises that melamine and formaldehyde maybe can provide the compound of methylene bridge to carry out condensation and the amino resins that forms.Alkyd resins and/or vinyl and melamine resin the staggered typical case that links to each other is embodied on the support pad discharging coating layer 135, needs dry or generation when solidifying.In one embodiment, with solid-state calculating, release coat comprises 0 to about 80wt.% and about in one embodiment 10 to about 30wt.% alkyd resins; Comprise 0 to about 80wt.% and about in one embodiment 10 to about 30wt.% vinyl; And comprise about 10 to about 30wt.% and about in one embodiment 20 to about 25wt.% melamine resin.
Discharge coating layer 135 and can comprise one or more solid particulate matters, these particles protrude into the surface 114 of dry paint rete 110, the surface 141 or the printed decoration layer 165 of transparent film layer 140, provide inferior light facing or plane facing to layer 110,140 or 165.When having particle, discharge coating layer 135 and can be called as matsurface releasing layer or matsurface release coat.Available particle is the above-mentioned any extender pigment that the coating rete uses that is used for.Object lesson comprises mica and alumina silicate.Can use the particle of irregular shape (as strip).By controlling the use of these particles, can control the configuration of surface of dry paint film layer, transparent film layer or printed decoration layer.For example, by using these particles, can carry out light face or semi-glossy arrangement to dry paint rete, transparent film layer or printed decoration layer.If do not use or use less these particles, then dry paint rete, transparent film layer or printed decoration layer just are glossy surface.The range of particle shared weight ratio in resin or binding agent can reach about 1.1: 1, be about 0.7: 1 to about 1.1: 1 in one embodiment, be about 0.7: 1 to about 0.9: 1 in one embodiment, and be about 0.9: 1 to about 1.1: 1 in one embodiment.
In the illustrated embodiment of Fig. 1-9, favourable, discharging coating layer 135, separate required release force with dry paint rete 110, transparent film layer 140 or printed decoration layer 165 bigger than discharging coating layer 136 and viscous layer 120 and separating required release force.In the illustrated embodiment of Fig. 6, discharge coating layer 135 and separate required release force with dry paint rete 110 to separate required stripping release force with viscous layer 120 than release coat 176 big.In one embodiment, discharge coating layer 135 separate with dry paint rete 110, transparent film layer 140 or printed decoration layer 165 required release force be per two inches about 20 to about 180 grams (g/2in), be 30 to about 150g/2in in one embodiment, be 40 to about 120g/2in in one embodiment, be 50 to about 100g/2in in one embodiment, be 50 to about 90g/2in in one embodiment, be about 70 to about 90g/2in in one embodiment, and be about 50 to about 65g/2in in one embodiment.In one embodiment, release coating layer 136 or 176 separates required release force with adhesive layer 120 be 10 to about 150g/2in, be about 20 to about 150g/2in in one embodiment, be about 20 to about 90g/2in in one embodiment, be about 30 to about 150g/2in in one embodiment, be about 30 to about 100g/2in in one embodiment, and be about 30 to about 70g/2in in one embodiment.The method of testing of measuring release force relates to measurement 2 inches wide release coat pad is peeled off required power on layer 110,140 or 165 or from the adhesive coating ground, during operation to become 90 ° angle stretching release coat pad and dilatory with respect to layer or ground with the speed of 300 inches of per minutes.This test can at room temperature be carried out.
In the layer 110,120,135,136,140,176,180 and 190 each can adopt known technology to spread and dry and/or curing independently of one another.Used technology comprises the intaglio plate coating, reverse intaglio plate coating, hectograph intaglio plate coating, print roll coating (roll coating), brush, rotogravure formula printing (knife-over roll), metering rod-type (metering rod), reverse print roll coating, scraper (doctor knife), dip-coating, mould is coated with (die coating), slit die is coated with (slotdie coating), spraying, curtain coating (curtain coating), sliding be coated with (slide coating), sliding curtain coating (slide curtain coating), extruding is coated with, co-extrusion is coated with, the aniline brushing, lead stamp (letter press), rotary screen printing (rotary screen), flat serigraphy (flat screen) etc.In one embodiment, adhesive layer 120 is a formation of pressure-sensitive adhesive layer, and adopts the transfer layer platen press to apply.Decorative layer 150,160 and 165 the available known printing technology of enforcement comprise intaglio printing, aniline printing, tiffany printing (silk screen), ink jet printing etc.Spread finish after, layer is exposed under the ionization of thermal source or form known or the photochemistry non-ionising radiation carries out drying and/or curing.Drying of using or solidification temperature can change from about 115 ℃ to about 160 ℃, are about 140 ℃ to about 150 ℃ in one embodiment.Available radiation source comprises ultraviolet light and electron beam.Produce these dry and/equipment that solidifies thermal source or radiation source knows for those of ordinary skills.One or more layers can be extruded in the layer 110,120,140 and 180.Layer 110 and/or 180 can be extruded simultaneously with adhesive layer 120.In one embodiment, supporting layer 180 is extruded simultaneously with adhesive layer 120, then dry-coated material rete 110 is applied (as intaglio printing) on supporting layer 180.
Layer 110,140 or 180 comprises monofilm or multilayer film two-layer or that the adjacent co-extruded films of multilayer is formed independently of one another.For example, layer 110,140 or 180 can comprise the mixed layer of one deck polyolefin and one deck polyolefin and ethylene-vinyl yl acetate (EVA) copolymer.In one embodiment, layer 110,140 or 180 comprises three layers, and for example basic layer of polyolefin or core layer and on the top layer of basic layer or core layer both sides can comprise identical or different polymer blend.
Use as shown in figure 11 the separate type extruder or double molds formula extruder as shown in figure 12, the dry-coated bed of material or rete 110 or supporting layer 180 can be extruded simultaneously with viscous layer 120.See Figure 11, release liner 200 is opened forward by extrusion die 210 from rolling up 240, and here the coated with adhesive layer 120, and by extrusion die 220, supporting layer 180 here is painted on the adhesive layer 120 then.The composite extrusion rolling that forms collects, as collecting shown in the volume 250.See Figure 12, release liner 200 is during through two extrusion die 230, by coated with adhesive 120 and supporting layer 180 simultaneously.The composite extrusion rolling that forms collects, as collecting shown in the volume 250.When preparing the composite extrusion of desired amt, during same or diverse location carry out lock out operation, just can remove collecting volume 250, place and treat subsequent treatment (as coating, printing etc.), therefore have higher preparation flexibility.Alternatively, carry out same operation, composite extrusion can not collected and directly send to coating, printing etc.Dry-coated material rete 110 can be extruded simultaneously with adhesive 120, and process is the same.Disclosed PCT International Application PCT/US95/11807, PCT/US95/11733, PCT/US95/11734 and PCT/US95/11717 further describe the multi-mould method of operating of coating pressure sensitive adhesive layer and film forming layer on ground simultaneously, are hereby incorporated by.Polymeric membrane material of extruding simultaneously and cementitious compositions can be pure or are emulsion or non-aqueous solution.The acrylic PSA of emulsion and non-aqueous solution is existing open, and for example at patent US5, the existing description in 639,811 and 5,164,444 is incorporated herein its disclosure as a reference.When membrane material that adopts emulsion and/or cementitious compositions, by using patent US5,716,669 (LaRose etc.) describe and require Patent right method, in extruder, water is removed.In one embodiment, membrane material of extruding simultaneously and adhesive are the composition (as less than about 1wt.%) of not moisture substantially and/or solvent.The existence of water or solvent can cause occurring in the composite membrane aperture and bubble in the extrusion.Because steam causes that the space that exists in the film is called as " hygrochase seam ".
When while extruded polymer membrane material and adhesive, their hot melt viscosity can be in certain width or scope, this can produce the polymeric film material of continuous homogeneous and the composite membrane of adhesive, mixes mutually with adhesive with polymeric film material to avoid the occurring film defective in the co-extrusion process.Weigh with co-extrusion process medium shear rate, the hot melt viscosity of polymeric film material is about 0.07 to about 15 times of adhesive hot melt viscosity.Shear rate is about 100sec
-1To about 10000sec
-1This multiple can be about 1 to about 15, is about 1 to about 10 in one embodiment.The melt viscosity of also expecting polymeric film material and adhesive is similar under extrusion temperature.For example, when adhesive was traditional hotmelt, its extrusion temperature was about 150 ℃ to about 200 ℃, is about 175 ℃ to about 200 ℃ in one embodiment.The extrusion temperature of choosing the polymeric film material of using with this adhesive is lower than about 200 ℃, is about 150 ℃ to about 180 ℃ in one embodiment.
Dry-coated material transfer laminate shown in Figure 1 can will discharge on the lower surface 134 that coating layer 136 is implemented in backing pad 132 by using the aforementioned applications technology, solidify release coat then and make.The layer that discharges coating layer 136 heavily is about 0.1 to 1g/m
2(gsm), be about 0.25 to about 0.35gsm in one embodiment.Discharge 135 of coating layers and use aforementioned applications technology (as the intaglio plate coating) to be implemented on the upper surface 133 of backing pad 132, carry out drying or curing then.The layer that discharges coating layer 135 heavily is about 2.5 to 6.5gsm, is about 4.5 to about 5.5gsm in one embodiment.The liquid coating or the coating composition that adopt aforementioned applications technology (as reverse roll banding, slit extrusion) will form dry paint rete 110 then are implemented in the surface that discharges coating layer 135, carry out drying or curing again.The layer of dry paint rete 110 heavily is about 20 to about 60gsm, is about 30 to about 40gsm in one embodiment.Can implement one or more layers.Adopt aforementioned applications technology (as the slit extrusion) that formation of pressure-sensitive adhesive layer 120 is implemented in the upper surface 112 of dry paint rete 110 then, carry out drying or curing.The enforcement of formation of pressure-sensitive adhesive layer can be used transfer laminate.The layer of formation of pressure-sensitive adhesive layer heavily is about 10 to 30gsm, is about 11 to about 17gsm in one embodiment.Dry-coated material transfer laminate 100 can be with known technology coiled web-like, as shown in Figure 2.
The preparation process of dry-coated material transfer laminate 100A shown in Figure 3 is identical with dry-coated material transfer laminate 100, just before implementing dry paint rete 110, implements transparent film layer 140 on coating layer 135 surfaces discharging earlier, and carries out drying or curing.Again dry paint rete 110 is implemented in transparent film layer 140 surfaces.The enforcement of transparent film layer 140 can be adopted one of aforementioned applications technology (as the intaglio plate coating).The layer of transparent film layer 140 heavily is about 1 to about 5gsm, is about 2.5 to about 3.5gsm in one embodiment.Can implement one or more layers.Dry-coated material transfer laminate 100A can use known technology coiled web-like as shown in Figure 2.
The preparation process of dry-coated material transfer laminate 100B shown in Figure 4 is identical with laminated material 100A, and just before implementing dry paint rete 110, the liquid coating composition that will form printed decoration layer 150 earlier is implemented in transparent film layer 140 surfaces and curing.Again dry paint rete 110 is implemented in printed decoration layer 150 surface.The enforcement of printed decoration layer 150 can be adopted aforementioned any printing technology (as intaglio printing, aniline printing, tiffany printing, ink jet printing etc.).The layer of printed decoration layer 150 heavily is about 0.3 to about 2gsm, is about 0.3 to about 0.7gsm in one embodiment.Dry-coated material transfer laminate 100B can use known technology coiled web-like as shown in Figure 2.
The preparation process of dry-coated material transfer laminate 100C shown in Figure 5 is identical with laminated material 100B, be before implementing printed decoration layer 150, the liquid coating composition that will form the second printed decoration layer 160 earlier is implemented in transparent film layer 140 surfaces and dry or curing.Implement printed decoration layer 150 on the surface of the second printed decoration layer 160 then.The enforcement of the second printed decoration layer 160 can be adopted aforementioned any printing technology (as intaglio printing, aniline printing, tiffany printing, ink jet printing etc.).The layer of the second printed decoration layer 160 heavily is about 0.3 to about 2gsm, is about 0.3 to about 0.7gsm in one embodiment.Dry-coated material transfer laminate 100C can use known technology coiled web-like as shown in Figure 2.
The preparation process of dry-coated material transfer laminate 100D shown in Figure 6 is identical with laminated material 100 among Fig. 1, and just release liner 170 bonds with adhesive layer 120, and release coat 176 contacts with adhesive layer 120.
The preparation process of dry-coated material transfer laminate 100E shown in Figure 7 is identical with laminated material 100 among Fig. 1, and just supporting layer 180 connects with dry-coated material rete 110.Supporting layer 180 can together be extruded with adhesive layer 120, then dry paint rete 110 is coated in (as the intaglio plate coating) on the supporting layer 180.Dry-coated material transfer laminate 100E can use known technology coiled web-like as shown in Figure 2.
The preparation process of dry-coated material transfer laminate 100F shown in Figure 8 is identical with laminated material 100 among Fig. 1, just coats separation layer 190 on dry paint rete 110.Dry-coated material transfer laminate 100F can use known technology coiled web-like as shown in Figure 2.
The preparation process of dry-coated material transfer laminate 100G shown in Figure 9 is identical with laminated material 100 among Fig. 1, and just supporting layer 180 connects with dry paint rete 110.Supporting layer 180 can together be extruded with adhesive layer 120.Printed decoration layer 150,160 and 165 sequentially is coated on the dry paint rete 110.Dry-coated material transfer laminate 100G can use known technology coiled web-like as shown in Figure 2.
The preparation process of dry-coated material transfer laminate 100H shown in Figure 10 is identical with laminated material 100C among Fig. 5, and just the used release liner of laminated material 100C is removed, and adds release liner 170 and releasing layer thereof.Dry paint rete 110 and adhesive layer 120 are together extruded on the releasing layer 176 of release liner 170.
The preparation of dry-coated material transfer laminate of the present invention can be used a production line or many production lines or overlap production equipment more.For many production lines or overlap for the production equipment, the part laminated material can be made into web-like more, and is dry or solidify, roll, and is transported to next production line or equipment, opens again, further handles, adds other layer.For example, dry paint rete 110 and viscous layer 120 can be attached long-pending on many production lines, or order is attached long-pending on a production line, or simultaneously attached long-pending as adopting co-extrusion or multi-mould coating process.The wall scroll Production Line does not have more efficient owing to having extra operation, deposit and transport step, and product comprises relatively thin and exquisiter membrane material at least in one embodiment.
When using dry-coated material transfer laminate 100, scroll laminated material shown in Figure 2 is opened, simultaneously laminated material is implemented on the ground (as wall) that will cover.Ground comprises any flat surfaces.Flat surfaces comprises building board, plastic plate, metallic plate, composite plate etc.Ground comprises inner surface (as indoor) or outer surface (as outdoor).Laminated material is placed on the ground, and its adhesive layer 120 contacts with ground.After release liner 130 was peeled off, dry paint rete 110 was by adhesive layer 120 and ground bonding.At least in one embodiment, use the advantage of this laminated material to be that can there be the slit in the dry paint rete of implementing substantially with the adjacent dry paint film ply of implementing next time, thereby merge into background.This advantage exist to small part be since dry paint rete 110 thinner.The glossiness of dry paint rete 110 and opacity also help to hide the slit.
The occupation mode of dry-coated material transfer laminate 100A on ground is identical with laminated material 100.When peeling off release liner 130, dry paint rete 110, transparent film layer 140 and adhesive layer 120 still bond with ground, and adhesive layer 120 contacts with ground.
The occupation mode of dry-coated material transfer laminate 100B on ground is identical with laminated material 100.When peeling off release liner 130, dry paint rete 110, printed decoration layer 150, transparent film layer 140 and adhesive layer 120 still bond with ground, and adhesive layer 120 contacts with ground.
The occupation mode of dry-coated material transfer laminate 100C on ground is identical with laminated material 100.When peeling off release liner 130, layer 110,150 and 160, transparent film layer 140 and adhesive layer 120 still bond with ground, and adhesive layer 120 contacts with ground.
The occupation mode of dry-coated material transfer laminate 100D on ground is identical with laminated material 100, and just laminated material is favourable writing board shape rather than web-like, and release liner 170 peels off before adhesive layer 120 and ground bond.
When dry-coated material transfer laminate 100E was implemented on the ground, adhesive layer 120 and ground bonding peeled off release liner 130 then.
When dry-coated material transfer laminate 100F implemented on the ground, adhesive layer 120 and ground bonding peeled off release liner 130 then.
When laminated material 100G was implemented on the ground, adhesive layer 120 and ground bonding peeled off release liner 130 then.
When laminated material 100H is implemented on the ground, peel off release liner 170 and release coat 176 thereof from laminated material earlier, again with adhesive layer 120 and ground bonding.When adopting laminated material, use proprietary utensil with release liner 170 and release coat 176 thereof around rising or roll, and the laminated material remainder is stayed on the ground.
Embodiment 1 and 2
Coating the silicone release coat that discharges coating layer 136 corresponding to second corresponding to the one side of the polyethylene terephthalate film support pad of backing pad 132.The thickness of release coat pad is 0.92 mil.
Adopt intaglio plate coating (gravure), coat the matsurface release coat that discharges coating layer 135 corresponding to first at the supporting pad another side, coating heavily is 6.5-7.75gsm.The prescription of matsurface release coat is as follows: the 26wt.% methyl iso-butyl ketone (MIBK), the 6wt.% isopropyl alcohol, 34.8wt.%Lankyd13-1425 (Akzo Resins product, be accredited as a kind of acrylic acid modified alkyd resins), 2.6wt.%Elvacite 2042 (Lucite International product, be accredited as a kind of polyethylene methacrylate ester polymer), 30wt.%Microtalc MP 15-38 (Barret ' s Minerals product, be accredited as a kind of mica intermixture pigment), 2.5wt.%Cycat 4040 is (by a kind of product of Cytec supply, be accredited as a kind of p-methyl benzenesulfonic acid (paratoluene sulfonic acid)) and 8.7wt.%Cymel 303 (a kind of product by the Cytec supply is accredited as a kind of melmac).Under 149 ℃ temperature, use powerful hot-air dry raw exasperate release coat.
Adopt the intaglio plate coating, coat the hyaline layer corresponding to hyaline layer or rete 140 on the matsurface release coat, the heavy 2.7-2.9gsm of coating under 120 ℃ temperature, uses powerful hot-air to carry out drying.The prescription of transparent film layer is as follows: 46.7wt.% butanone, 31.3wt.% toluene, 11wt.%VYNS (Union Carbide product, be accredited as a kind of vinyl chloride/vinyl acetate copolymer, contain the 5-20wt.% vinylacetate) and 11wt.%Vitel 2200B (the Bostic product is accredited as polyester copolymer).
Following coating composition is used for forming the dry-coated bed of material corresponding to the dry-coated bed of material or rete 110 on transparent film layer, one is used for embodiment 1, and another is used for embodiment 2.Embodiment 1 is a dark brown, and embodiment 2 is greenish orange look.In the following table, all numerical value are weight portion.
Embodiment 1 | Embodiment 2 | |
Butanone toluene VYHH (Union Carbide product; Be accredited as a kind of vinyl chloride/vinyl acetate copolymer) Edinol 9790 (the Cognis product is accredited as the polyester plasticizer) yellow uitramarine 42 (iron oxide) orange pigment 36 (monoazo benzimidazole) black 7 (carbon black) white 6 (titanium dioxide) | 66.7 33.3 50.05 24.65 17.8 2.5 0.1 4.9 | 66.7 33.3 30.55 15.05 2.3 0.38 0.02 51.7 |
Pigment volume ratio is 10% among the embodiment 1, and embodiment 2 is 27%.Aforementioned coating composition is coated on the hyaline layer with reverse roll banding coating machine, carries out drying to drive solvent under 135 ℃.The build of each dry-coated bed of material is 0.7 mil.
Adopt the mobile layer platen press then, coloured formation of pressure-sensitive adhesive layer is coated on the dry-coated bed of material, the heavy 14-20gsm of coating so just has the adhesive layer corresponding to formation of pressure-sensitive adhesive layer 120.The prescription of formation of pressure-sensitive adhesive layer is as follows: 70-90wt.%2-ethylhexyl acrylate, 1-10wt.% acrylic acid, 10-20wt.% methacrylate, 3.7wt.%UCD 1106E (Rohm and Hass product, be accredited as titanium dioxide and disperse condensation product) and 0.3wt.%UCD 1507E (Rohmand Hass product is accredited as carbon black and disperses condensation product).
Embodiment 3
Repeat the process of embodiment 1 and 2, only be to use following liquid coating composition, form the dry-coated bed of material corresponding to the dry-coated bed of material or rete 110.In the following table, all numerical value are weight portion.
Butanone 29.6
Toluene 19.5
Vitel 2200B 11.6
(the Bostic product is accredited as polyethylene terephthalate copolymer 11.5 to Vitel 2650
Thing)
R-900 (the DuPont product is accredited as titanium dioxide) 27.5
955-39230 (Gibraltar ChemicalWorks product, 0.2
Be accredited as and block black (shading black))
99-34520 (Gibraltar ChemicalWorks product, 0.1
Be accredited as phthalocyanine blue GS)
955-37470 (Gibraltar ChemicalWorks product, the amount that does not almost recognize is accredited as the carbazole violet rowland)
Aforementioned coating composition is light blue.The build of dry paint rete is the 0.6-0.8 mil.
Embodiment 4
Coating the silicone release coat that discharges coating layer 136 corresponding to second corresponding to the one side of the polyethylene terephthalate film support pad of backing pad 132.The thickness of release coat pad is 0.92 mil.
Adopt the intaglio plate coating, coat the matsurface release coat that discharges coating layer 135 corresponding to first at the supporting pad another side, coating heavily is 4.4-4.6gsm.The prescription of matsurface release coat is as follows: 50.54wt.% methyl iso-butyl ketone (MIBK), 7.84wt.% isopropyl alcohol, 8.93wt.%Lankyd 13-1425,10.68wt.%VAGH (Union Carbide product is accredited as the polyvinyl chloride/polyvinylacetate copolymer of hydroxyl modification), 22wt.%Microtalc MP 15-38,2wt.%Cycat 4040 and 6.8wt.%Cymel 303.Dry raw exasperate release coat under 149 ℃, powerful hot-air.
Adopt the intaglio plate coating, coat the ground floor hyaline layer corresponding to hyaline layer 140 on the matsurface release coat, the heavy 1.3-2gsm of coating carries out drying under 120 ℃, powerful hot-air.The thickness of desciccator diaphragm is the 0.05-0.1 mil.The prescription of ground floor hyaline layer is as follows: 41.5wt.% butanone, 41.5wt.% methyl iso-butyl ketone (MIBK) and 17wt.%Elvacite 2024 (Lucite International product is accredited as polymethyl methacrylate).
Adopt the intaglio plate coating, coat the second layer transparent film layer corresponding to hyaline layer or rete 140 on the ground floor hyaline layer, the heavy 1.0-1.5gsm of coating carries out drying under 120 ℃, powerful hot-air.The thickness of desciccator diaphragm is the 0.03-0.7 mil.The prescription of second layer hyaline layer is as follows: 41.5wt.% butanone, 41.5wt.% methyl iso-butyl ketone (MIBK) and 17wt.%VYHH (Union Carbide product is accredited as a kind of vinyl chloride/vinyl acetate copolymer, contains the 5-20wt.% vinylacetate).
At the decorative layer that prints on the second layer transparent film layer corresponding to printed decoration layer 160, the heavy 3.0-3.2gsm of coating carries out drying under 120 ℃, powerful hot-air.The coating composition that is used for this decorative layer has following prescription (all numerical value are weight portion):
Butanone 42.6
Methyl iso-butyl ketone (MIBK) 38.7
VYHH 15.86
DP 80110 (Gibraltar Chemical Works product, 2.1
Be accredited as and contain butanone, toluene, carbon black and acrylate copolymer)
DP 36640 (Gibraltar Chemical Works product, 0.22
Be accredited as and contain butanone, toluene, the red and acrylic acid of quinoline a word used for translation diketone
Polymer)
18977 (Gibraltar Chemical Works product, 0.10
Be accredited as and contain butanone, toluene, R.S. phthalocyanine blue and acrylate copolymer)
18980 (Gibraltar Chemical Works product, 0.38
Be accredited as and contain butanone, toluene, isoindolinone Huang and acrylate copolymer)
Above-mentioned corresponding to the decorative layer of the second printed decoration layer 160 on printing corresponding to the decorative layer of printed decoration layer 150, the heavy 0.8gsm of coating carries out drying under 120 ℃, powerful hot-air.The coating composition that is used for this decorative layer has following prescription (all numerical value are weight portion):
Butanone 42.85
Methyl iso-butyl ketone (MIBK) 39.1
VYHH 16.0
DP 80110 1.71
DP 36640 0.18
18977 0.18
Following coating composition is coated on the above-mentioned decorative layer corresponding to printed decoration layer 150, and the heavy 30-32gsm of coating carries out drying, thereby obtains the dry paint rete corresponding to the dry-coated bed of material or rete 110 under 120 ℃, hot-air.In the following table, all numerical value are weight portion.
Butanone 34
Toluene 16.7
VYHH 18.3
Edinol 9790 9
AVI-0301-3 orange (Gibraltar Chemical Works product, 8.9
Be accredited as and contain butanone, toluene, diaryl orange, VYHH and Edinol 9790)
AVI-0301-5 fuchsin (Gibraltar Chemical Works product, 5.3
Be accredited as and contain butanone, toluene, metal azophloxine, VYHH and Edinol 9790)
AVI-0301-6 iron oxide red (Gibraltar Chemical Works product, 3.7
Be accredited as and contain butanone, toluene, iron oxide red, VYHH and Edinol 9790)
AVI-0301-1 TiO
2(Gibraltar Chemical Works produces 3.52 in vain
Product,
Be accredited as and contain butanone, toluene, titanium dioxide, VYHH and Edinol 9790)
AVI-0301-2 carbon black (Gibraltar Chemical Works product, 0.03
Be accredited as and contain butanone, toluene, carbon black, VYHH and Edinol9790)
Adopt the mobile layer platen press then, coloured formation of pressure-sensitive adhesive layer is coated on the dry-coated bed of material corresponding to the dry-coated bed of material or rete 110, the heavy 17gsm of coating so just has the adhesive layer corresponding to formation of pressure-sensitive adhesive layer 120.The prescription of formation of pressure-sensitive adhesive layer is as follows: 96wt.% contains the weak adhesive propylene yogurt glue, 3.7wt.%UCD 1106E and the 0.3wt.%UCD 1507E that are cross-linked copolymer of butyl acrylate and EHA.
Embodiment 5
Coating the silicone release coat that discharges coating layer 136 corresponding to second corresponding to the one side of the polyethylene terephthalate film support pad of backing pad 132.The thickness of release coat pad is 0.92 mil.
Adopt the intaglio plate coating, coat the matsurface release coat that discharges coating layer 135 corresponding to first at the supporting pad another side, coating heavily is 4.4-4.6gsm.Dry raw exasperate release coat under 149 ℃, powerful hot-air.The prescription of matsurface release coat following (all numerical value are weight portion):
Methyl iso-butyl ketone (MIBK) 52.54
Elvacite 4402 (Lucite International product, 20.98
A kind of acrylic resin of hydroxyethyl methacrylate modification)
VYNS 1.35
Microtalc 15-38 22.85
Byk 451 (Byk Chemie product, 2.2
Block acid catalyst)
Cymel 303 6.38
Adopt reverse roll-type coating machine, coat the hyaline layer corresponding to hyaline layer or rete 140 on the matsurface release coat, the heavy 13gsm of coating carries out drying under 120 ℃, powerful hot-air.The thickness of dry film is 0.4 mil.The prescription of transparent film layer following (all numerical value are weight portion):
Rucothane CO-A-5002L (Ruco Chemical product, 62.5
Be accredited as polyester urethane)
Toluene 18.75
Isopropyl alcohol 18.75
Printing is corresponding to the decorative layer of printed decoration layer 150 on above-mentioned transparent film layer, and coating heavily is 1gsm, carries out drying under 120 ℃, hot-air.The coating composition that is used for this decorative layer has following prescription (all numerical value are weight portion):
Butanone 25.67
Methyl iso-butyl ketone (MIBK) 22.0
VYHH 9.17
18980 3.5
DP 37251 (Gibraltar Chemical Works product, 0.99
Be accredited as contain that perylene is red, butanone, toluene and acrylate copolymer)
DP 80110 1.0
DP 39600 (Gibraltar Chemical Works product, 37.47
Be accredited as and contain TiO
2, butanone, toluene and acrylate copolymer)
18977 0.20
Following coating composition is coated on the above-mentioned decorative layer corresponding to printed decoration layer 150, and the heavy 66gsm of coating carries out drying, thereby obtains the dry paint rete corresponding to dry paint rete 110 under 138 ℃, hot-air.In the following table, all numerical value are weight portion:
Methylisobutylketone 24.11
Toluene 20.65
VYHH 11.54
R-900 38.4
(Rohm and Hass product is accredited as 3.86 to Acroloid B-72
A kind of acrylic resin)
18980 2.6
DP37251 0.21
DP80110 0.40
Adopt the mobile layer platen press then, formation of pressure-sensitive adhesive layer is coated on the dry-coated bed of material corresponding to the dry-coated bed of material or rete 110, the heavy 15-20gsm of coating so just has the adhesive layer corresponding to formation of pressure-sensitive adhesive layer 120.Formation of pressure-sensitive adhesive layer is the acrylic based emulsion of weak viscosity.The prescription of formation of pressure-sensitive adhesive layer is as follows: 70-90wt.%2-EHA, 1-10wt.% acrylic acid and 10-20wt.% methyl acrylate.
Embodiment 6
Coating the silicone release coat that discharges coating layer 136 corresponding to second corresponding to the one side of the polyethylene terephthalate film support pad of backing pad 132.The thickness of release coat pad is 0.92 mil.
Adopt the intaglio plate coating, coat corresponding to the matsurface release coat that discharges coating layer 135 at the supporting pad another side.Dry raw exasperate release coat under 148.9 ℃, powerful hot-air.The layer of matsurface release coat heavily is 4.0-5.0gsm.The prescription of matsurface release coat following (all numerical value are weight portion):
Methyl iso-butyl ketone (MIBK) 42.03
Isopropyl alcohol 8.51
Microtalc 15-38 23.87
Cymel 303 7.36
Cycat 4040 1.8
VROH (Union Carbide product, 16.43
Be accredited as the vinyl chloride/vinyl acetate copolymer of band OH functional group)
Use 2 mil Byrd rods (byrd bar), coat the hyaline layer corresponding to hyaline layer or rete 140 on the second matsurface release coat, the heavy 30gsm of coating carries out drying under 126.7 ℃, hot-air.The prescription of transparent film layer following (all numerical value are weight portion):
Water 7.98
N-methyl pyrrolidone 4.79
Texanol (Eastman Chemical product, 4.79
Be accredited as a kind of alcohol ester)
BYK 333 (Byk Chemie product, 0.4
Be accredited as wetting agent)
Vycar 351 (Noveon product, 79.81
Be accredited as the polyvinyl chloride copolymer latex)
Antifoam PD-218 (Magrabar Chemical product, 0.32
Be accredited as defoamer)
Rheolate 350 (Rheox company product is accredited as thickener) 1.92
Following coating composition is coated on the above-mentioned hyaline membrane, and the heavy 96gsm of coating under 126.7 ℃, uses hot-air to carry out drying, thereby obtains the dry paint rete corresponding to the dry-coated bed of material or rete 110.In the following table, all numerical value are weight portion:
Water 18.28
Surfynol CT-324 (Air Products product, 0.98
Be accredited as surfactant)
R-900 32.88
Vycar 460 * 45 (Noveon product, 34.72
Be accredited as vinyl chloride/acrylic copolymer)
Vycar 460 * 46 (Noveon product, 11.57
Be accredited as vinyl chloride/acrylic copolymer)
Antifoam PD-218 0.19
BYK 333 0.23
Rheolate 350 1.2
Adopt the mobile layer platen press then, formation of pressure-sensitive adhesive layer is coated on the dry paint rete corresponding to the dry-coated bed of material 110, the heavy 17gsm of coating so just has the adhesive layer corresponding to formation of pressure-sensitive adhesive layer 120.The prescription of formation of pressure-sensitive adhesive layer is as follows: 96wt.% contains the weak viscosity latex, 3.7wt.%UCD 1106E and the 0.3wt.%UCD 1507E that are cross-linked copolymer of butyl acrylate and EHA.
Embodiment 7
Coating the silicone release coat that discharges coating layer 136 corresponding to second corresponding to the one side of the polyethylene terephthalate film support pad of backing pad 132.The thickness of release coat pad is 0.92 mil.
Adopt the intaglio plate coating, coat the matsurface release coat that discharges coating layer 135 corresponding to first at the supporting pad another side, coating heavily is 4.4-4.6gsm.The prescription of matsurface release coat is as follows: 50.54wt.% methyl iso-butyl ketone (MIBK), 7.84wt.% isopropyl alcohol, 8.93wt.%Lankyd 13-1425,10.68wt.%VAGH (Union Carbide product, the polyvinyl chloride of hydroxyl modification/polyvinylacetate copolymer), 22wt.%Microtalc MP 15-38,2wt.%Cycat 4040 and 6.8wt.%Cymel 303.Dry raw exasperate release coat under 149 ℃, powerful hot-air.
Adopt the intaglio plate coating, coat the hyaline layer corresponding to hyaline layer or rete 140 on the matsurface release coat, the heavy 12-16gsm of coating carries out drying under 165 ℃, powerful hot-air.The thickness of dry film is the 0.35-0.5 mil.The prescription of transparent film layer following (all numerical value are weight portion):
Cyclohexanone 69.3
Elvacite 2042 10.5
Solsperse 17000 (the Avecia product is accredited as wetting agent) 0.1
Tinuvin 234 (the Ciba product is accredited as light stabilizer) 0.6
(the Atofina product is accredited as polyvinyl fluoride equal 27.0 to Kynar 301F
Polymers)
N-N-methyl-2-2-pyrrolidone N-2.5
Printing is corresponding to the decorative layer of the second printed decoration layer 160 on clear coat, and the heavy 0.3-1.2gsm of coating carries out drying under 105 ℃, hot-air.The coating composition that is used for this decorative layer has following prescription (all numerical value are weight portion):
Butanone 36.0
Methyl propyl ketone 35.1
(the Atofina product is accredited as poly-fluorine 10.2 to Kynar 7201 (SL)
Ethylene copolymer)
(Lucite International product is identified 3.4 to Elvacite 2010
Be polymethyl methacrylate)
Tinuvin 234 0.27
DP35740 (Gibraltar Chemical Works product, 0.10
Be accredited as light yellow mixed-metal oxides pigment condensation product)
DP35820 (Gibraltar Chemical Works product, 11.7
Be accredited as brown mixed-metal oxides pigment condensation product)
DP39040 (Gibraltar Chemical Works product, 3.3
Be accredited as black mixed-metal oxides pigment condensation product)
Above-mentioned corresponding to the decorative layer of the second printed decoration layer 160 on printing corresponding to the decorative layer of printed decoration layer 150, the heavy 0.3-1.2gsm of coating carries out drying under 105 ℃, hot-air.The coating composition that is used for this decorative layer has following prescription (all numerical value are weight portion):
Butanone 34.0
Methyl propyl ketone 33.0
Kynar 7201(SL) 9.6
Elvacite 2010 3.2
Tinuvin 234 0.25
DP35740 14.4
DP35820 5.0
DP39040 3.2
Following coating composition is coated on the above-mentioned decorative layer corresponding to printed decoration layer 150, and the heavy 6-10gsm of coating carries out drying, thereby obtains the dry-coated bed of material corresponding to the dry-coated bed of material or rete 110 under 105 ℃, hot-air.In the following table, all numerical value are weight portion.
Butanone 27.6
Methyl propyl ketone 26.3
Kynar 7201(SL) 7.4
Elvacite 2010 2.5
Tinuvin 234 0.2
DP35740 4.1
DP35820 7.8
DP39040 0.6
DP39600 (Gibraltar Chemical Works product, 23.6
Be accredited as white TiO 2 pigment condensation product)
Adopt mobile layer platen press (transfer lamination) then, coloured formation of pressure-sensitive adhesive layer is coated on the dry paint rete corresponding to dry paint rete 110, the heavy 17gsm of coating so just has the adhesive layer corresponding to formation of pressure-sensitive adhesive layer 120.The prescription of formation of pressure-sensitive adhesive layer is as follows: 96wt.% contains the weak adhesive propylene yogurt glue, 3.7wt.%UCD 1106E and the 0.3wt.%UCD 1507E that are cross-linked copolymer of butyl acrylate and EHA.
Embodiment 8
Coating the silicone release coat that discharges coating layer 136 corresponding to second corresponding to the one side of the polyethylene terephthalate film support pad of backing pad 132.The thickness of release coat pad is 0.92 mil.
Adopt the intaglio plate coating, coat the matsurface release coat that discharges coating layer 135 corresponding to first at the supporting pad another side, coating heavily is 4.4-4.6gsm.The prescription of matsurface release coat is as follows: 50.54wt.% methyl iso-butyl ketone (MIBK), 7.84wt.% isopropyl alcohol, 8.93wt.%Lankyd13-1425,10.68wt.%VAGH (Union Carbide product, the polyvinyl chloride of hydroxyl modification/polyvinylacetate copolymer), 22wt.%Microtalc MP 15-38,2wt.%Cycat 4040 and 6.8wt.%Cymel 303.Dry raw exasperate release coat under 149 ℃, powerful hot-air.
Printing is corresponding to the decorative layer of the second printed decoration layer 160 on the matsurface release coat, and the heavy 0.3-1.2gsm of coating carries out drying under 105 ℃, hot-air.The coating composition that is used for this decorative layer has following prescription (all numerical value are weight portion):
Butanone 36.0
Methyl propyl ketone 35.1
(the Atofina product is accredited as poly-fluorine 10.2 to Kynar 7201 (SL)
Ethylene copolymer)
(Lucite International product is identified 3.4 to Elvacite 2010
Be polymethyl methacrylate)
Tinuvin 234 0.27
DP35740 (Gibraltar Chemical Works product, 0.10
Be accredited as light yellow mixed-metal oxides pigment condensation product)
DP35820 (Gibraltar Chemical Works product, 11.7
Be accredited as brown mixed-metal oxides pigment condensation product)
DP39040 (Gibraltar Chemical Works product, 3.3
Be accredited as black mixed-metal oxides pigment condensation product)
Above-mentioned corresponding to the decorative layer of the second printed decoration layer 160 on printing corresponding to the decorative layer of printed decoration layer 150, the heavy 0.3-1.2gsm of coating carries out drying under 105 ℃, hot-air.The coating composition that is used for this decorative layer has following prescription (all numerical value are weight portion):
Butanone 34.0
Methyl propyl ketone 33.0
Kynar 7201(SL) 9.6
Elvacite 2010 3.2
Tinuvin 234 0.25
DP35740 14.4
DP35820 5.0
DP39040 3.2
Adopt rotogravure coating (rotogravure), following coating composition is coated on the above-mentioned decorative layer corresponding to printed decoration layer 150, the heavy 5-16gsm of coating carries out drying, thereby obtains the dry-coated material rete corresponding to the dry-coated bed of material 110 under 105 ℃, hot-air.In the following table, all numerical value are weight portion.
Toluene 19.0
Butanone 23.6
VYHH 5.8
Ednol 9790 2.9
DV39600 (Gibraltar Chemical Works product, 48.6
Be accredited as the ferric oxide red colorant dispersion)
DV39420 (Gibraltar Chemical Works product, 0.07
Be accredited as the carbon black pigment dispersion)
DV36500 (Gibraltar Chemical Works product, 0.03
Be accredited as Pigment Red pigment dispersion)
DV34130 (Gibraltar Chemical Works product, 0.10
Be accredited as Phtalo Blue RS pigment dispersion)
Adopt print roll coating method (roll coating), on above-mentioned dry paint rete, be coated with the coating composition of top and bottom, coating heavily be 20-30gsm, carries out drying in 105 ℃, hot-air, and formation is corresponding to the supporting layer of supporting layer 180.In table, all numerical value are weight portion.
Toluene 14.1
Butanone 21.1
VYHH 13.2
Ednol 9790 6.6
DV39600 44.96
DV39420 0.07
Adopt the mobile layer platen press then, coloured formation of pressure-sensitive adhesive layer is coated on the coating corresponding to supporting layer 180, the heavy 17gsm of coating so just has the adhesive layer corresponding to formation of pressure-sensitive adhesive layer 120.The prescription of formation of pressure-sensitive adhesive layer is as follows: 96wt.% contains the weak adhesive propylene yogurt glue, 3.7wt.%UCD1106E and the 0.3wt.%UCD 1507E that are cross-linked copolymer of butyl acrylate and EHA.
Though, the present invention is illustrated, should be appreciated that concerning the those of ordinary skills that read this specification it is done various modifications is obviously feasible in conjunction with embodiment preferred.Therefore, should be appreciated that invention disclosed herein comprises these modifications, belong to claim category of the present invention.
Claims (62)
1. dry-coated material transfer laminate comprises:
The dry-coated bed of material, it contains color layers, and color layers comprises base-material and pigment, and the described dry-coated bed of material has upper surface and lower surface;
Formation of pressure-sensitive adhesive layer covers the upper surface of the described dry-coated bed of material; With
Release liner, adhere to the lower surface of the described dry-coated bed of material releasedly, described release liner has the carrying release coat, the carrying release coat comprises particle, described particle protrudes and enters in the dry-coated bed of material that adheres to releasedly, make when adhesive layer exerting pressure time adhere to laminated material in the substrate and release liner by when the dry-coated bed of material divests, coarse facing is transferred on the exposed surface of the dry-coated bed of material.
2. the laminated material of claim 1, wherein said release liner further comprises: the adhesive release coat is positioned at the side, relative with the carrying release coat of described liner.
3. the laminated material of claim 1, the wherein said dry-coated bed of material comprises at the color layers of the dry-coated bed of material and the hyaline layer between the release liner, and therein, described carrying release coat is to adhere on the hyaline layer releasedly.
4. the described laminated material of claim 1,2 or 3, the wherein said dry-coated bed of material comprises the printed decoration layer, be positioned at color layers a side, close on described release liner.
5. the laminated material of claim 1, wherein said base-material comprises one or more acrylic resins, vinyl, mylar, alkyd resins, butadiene resin, styrene resin, phthalic acid or anhydride resin, polyurethane resin, epoxy resin, fluoropolymer resin, or contain the polymer or the copolymer of ethene or propylene units.
6. the laminated material of claim 1, the wherein said dry-coated bed of material is derived from fluid composition, and fluid composition contains water or water-alcohol mixture or organic solvent.
7. the laminated material of claim 3, wherein said hyaline layer comprises acrylic materials, and described color layers comprises plasticizing vinyl material.
8. the laminated material of claim 1, wherein said adhesive comprises rubber based adhesives, acrylic acid adhesive, the vinethene adhesive, silicone adhesive stick, or wherein the two or multiple mixture, and wherein said adhesive layer is derived from heat sealing adhesive, organic solvent base adhesive, or water accack.
9. any described laminated material of aforementioned claim, wherein said carrying release coat comprises alkyd resins and/or vinyl, and is crosslinked with melmac.
10. the laminated material of claim 2, wherein said adhesive release coat comprises silicone based material.
11. the laminated material of claim 2 has from roll form, therein, being used for separating the required release force of release coat from the dry-coated bed of material is greater than being used for from the required release force of adhesive layer separation gel stick release coat.
12. the laminated material of claim 2, have from roll form, therein, be used for the carrying release coat of release liner from the dry-coated bed of material separate required release force be per two inches from about 20 scopes to about 180 grams, two inches wide samples of wherein said release liner are to get off from the dry-coated bed of material is separated, are by being that 90 degree, speed are that the pulling of 300 inches of per minutes is carried out with angle.
13. the laminated material of claim 2 or 12, have from roll form, therein, be used for the carrying release coat of release liner from the dry-coated bed of material separate required release force be per two inches from about 30 scopes to about 150 grams, two inches wide samples of wherein said release liner are to get off from the dry-coated bed of material is separated, are by being that 90 degree, speed are that the pulling of 300 inches of per minutes is carried out with angle.
14. method that is used to prepare layer laminates, comprise: a side applying coatings layer and dope layer dry or that solidify on the release liner at release liner form the dry-coated bed of material, described release liner comprises thin and soft polymerization carrier film, described dope layer comprises base-material and pigment, and described release liner has the release surface that contacts with the described dry-coated bed of material; With at dope layer, the side coating formation of pressure-sensitive adhesive layer relative with release liner, be characterised in that following steps: coating matsurface release coat on release liner, described matsurface release coat comprises resin material, thereby resin material contains dispersed particles shape filler and at room temperature is sclerosis attitude formation rough surface, the dry-coated bed of material that contacts with rough surface with applying coatings layer and drying or curing on the rough surface of matsurface release coat, so that releasedly the dry-coated bed of material is adhered to rough surface, when laminated material is adhered to substrate and is removed release liner from it by formation of pressure-sensitive adhesive layer, rough surface can discharge from dry-coated bed of material adaptability at ambient temperature, the rough surface facing is transferred on the exposed surface of the dry-coated bed of material.
15. a dry-coated material transfer laminate comprises:
The matsurface release liner, the dried matsurface release coat that it contains soft polymerization carrier film and bonds with described carrier film;
The soft dry-coated bed of material contacts with matsurface release coat on the release liner releasedly;
With, dried adhesive layer bonds, is a side relative with matsurface release liner position in the one side with the dry-coated bed of material,
The described dry-coated bed of material comprises the pigment that is dispersed in the polymer base material,
Described matsurface release coat has adherence to a certain degree, and when adhesive one side that makes laminated material contacted with substrate, this can adhere to the matsurface release liner on the dry-coated bed of material releasedly, for laminated material provides support,
Described adhesive layer comprises pressure-sensitive adhesive, is used at ambient temperature, by applying pressure on the dry-coated material transfer laminate, the dry-coated bed of material is adhered in the substrate,
Described matsurface release coat comprises particle, and described particle protrudes and enters the dry-coated bed of material, makes when after laminated material and the substrate adhesion, when release liner and the dry-coated bed of material disengage, and coarse facing is transferred on the exposed surface of the dry-coated bed of material.
16. the laminated material of claim 15, the wherein said dry-coated bed of material comprises resin binder, and described resin binder comprises that vinylacetate/vinyl chloride copolymer or one or more are selected from the resin of acrylic acid, polyurethane, polyester, alkyd, butadiene, fluoropolymer polymer, polyolefin or vinyl.
17. the laminated material of claim 15, wherein said release coat is selected from vinyl, acrylic resin, mylar, alkyd resins, and vinyl chloride/vinyl acetate co-polymer.
18. the laminated material of claim 15, the wherein said dry-coated bed of material comprises painted color coating and clear coating layer, therein, clear coating layer is to be in the releasable contact condition with the matsurface release coat, and, therein, described clear coating layer comprises acrylic resin, and described color coating comprises the plasticizing vinyl.
19. the laminated material of claim 15, therein, described matsurface release coat comprises polymer base material, and particle is scattered in wherein, and therein, particle is from about 0.7 to 1.0 to about 1.1 to 1.0 with the ratio of resin binder.
20. a layer laminates comprises:
The dry-coated bed of material that comprises base-material and pigment, the described dry-coated bed of material has upper surface and lower surface;
Dry-pressing sensitive adhesive layer covers the upper surface of the dry-coated bed of material; With
Cover the release liner of the lower surface of the dry-coated bed of material, described release liner comprises matsurface release coat on thin and soft polymerization carrier film and the carrier film, that made by thermoset resin material, described matsurface release coat and described carrier film bonding form rough surface, when at ambient temperature when dope layer removes release liner, the rough surface facing is transferred to the dry-coated bed of material.
21. the laminated material of claim 20, wherein said matsurface release coat is selected from acrylic resin, mylar, alkyd resins, and vinyl chloride/vinyl acetate co-polymer.
22. the laminated material of claim 20, wherein said clear coating layer comprises acrylic resin, and described color coating comprises the plasticizing vinyl, and adhesive layer comprises crosslinked acrylic materials.
23. method that is used to prepare layer laminates, comprise the applying coatings layer to release liner, and dope layer dry or that solidify on the release liner form the dry-coated bed of material, described release liner comprises thin and soft polymerization carrier film, described dope layer comprises base-material and pigment, and described release liner has the release surface that contacts with the dry-coated bed of material; With the coating formation of pressure-sensitive adhesive layer to dope layer, a side relative with release liner, be characterised in that following step: coating thermosetting resin matsurface release coat to release liner, and at high temperature solidify release coat on the liner, the composition of described release coat material forms the bonding with release liner, and at room temperature form the matsurface release surface of hardening state, and under its hardening state, form the adherence of certain level; And the applying coatings layer is to rough surface and dry or solidify its above dope layer, described matsurface release coat adheres to the dry-coated bed of material releasedly, when laminated material be adhered on the substrate surface by formation of pressure-sensitive adhesive layer and release liner thereafter by when the dry-coated bed of material removes, at room temperature the transferring rough surface facing is to the dry-coated bed of material.
24. a layer laminates comprises:
The dry-coated bed of material, it contains color layers, and color layers comprises base-material and pigment, and the described dry-coated bed of material has upper surface and lower surface;
Dry-pressing sensitive adhesive layer is covered in the upper surface of the dry-coated bed of material; With
Release liner is covered in the lower surface of the dry-coated bed of material,
Matsurface release coat on described release liner comprises thin and soft polymerization carrier film and is positioned at carrier film, that contact with dry-coated bed of material tiling, described matsurface release coat is made by the resinous coat material that at room temperature is the attitude of hardening, wherein said coating material (1) forms rough surface, it adheres to the dry-coated bed of material releasedly, (2) at room temperature discharge from the dry-coated bed of material, (3) the transferring rough surface facing is being shifted when the dry-coated bed of material removes when release liner to the exposed surface of the dry-coated bed of material.
25. the laminated material of claim 24, wherein said release liner has upper surface and lower surface; Wherein said matsurface release coat covers the upper surface of release liner; And the lower surface of outer release coat covering release liner, make to contact with discharging of adhesive layer in roll form, forming of laminated material.
26. the laminated material of claim 24 or 25, wherein said laminated material further comprises the separation layer between the dry-coated bed of material and adhesive layer, and wherein said separation layer comprises polymer or the copolymer that contains acrylate, polyvinyl alcohol, the copolymer of ethene and vinylacetate, be derived from the copolymer of ethene, vinylacetate and polyvinyl alcohol, or be derived from the polymer blend of polyvinyl alcohol and polyurethane.
27. the laminated material of claim 24, wherein from the dry-coated bed of material separate the required described release force of release liner be per two inches about 20 to the scopes of about 180 grams, wherein two of release liner inches wide samples are to separate from the dry-coated bed of material, are that 90 degree, speed are that per minute spurs for 300 inches and separates with angle.
28. the laminated material of claim 24, wherein said release coat is included on the release liner and had been hardened already or the cured thermosetting material, described release coat material at room temperature, under its hard attitude condition, form the matsurface release surface, so that when release liner is removed on them, the rough surface facing is transferred on the dry-coated bed of material, and the glossiness that the rough surface facing has when 85 spend is less than 30%.
29. the laminated material of claim 28, contain the upper surface that is placed in the dry-coated bed of material and the hyaline layer between the release liner, wherein rough surface is transferred on the hyaline layer, and release coat comprises the solid particle that protrudes the surface enter hyaline layer, so that form rough surface.
30. a layer laminates comprises:
Have soft polymerization carrier film and with the release liner of the matsurface release coat of carrier film bonding, be adhered to the soft dry-coated material transfer layer on the matsurface release coat releasedly, with with the dry-pressing sensitive adhesive layer of dry-coated material transfer layer, relative side bonding with release liner, described dry-coated material transfer layer contains color layers, color layers comprises pigment, pigment is comprised in the polymerization base-material
Described matsurface release coat has the adherence of certain level, when adhesive one side of placing the dry-coated bed of material contacts with substrate, the matsurface release coat preferentially adheres to release liner dry-coated material transfer layer, is enough to provide for the dry-coated bed of material support structure of certain level
Described matsurface release coat comprises resin material, and described resin material had been hardened already or solidify to form little roughened surface, makes when release coat and the dry-coated bed of material disengage, and is used for the rough surface facing is transferred to the exposed surface of the dry-coated bed of material,
Described adhesive layer at room temperature has downtrod initial adherence level, this allow by after the dry-coated bed of material removes release liner, laminated material is adhered in the substrate, described adhesive layer experience is owing to the follow-up of adhesive effect due to the time lapse reason gathered, and is enough to make that the dry-coated bed of material and substrate are permanent combines.
31. laminated material according to claim 30, wherein from the matsurface release coat transfer to the dry-coated bed of material glossiness level 85 the degree under less than 30%.
32. laminated material according to claim 30, wherein said dry-coated material transfer layer contains the clear coating layer that covers on the color layers, and wherein said clear coating layer contacts with the matsurface release coat, is used to shift little roughened surface to clear coating layer.
33. laminated material according to claim 30, wherein said release liner comprises polyester film, and polyester film at room temperature is non-ductility substantially.
Strengthen the polymer support layer 34. laminated material according to claim 30, wherein said laminated material contain, between the dry-coated bed of material and adhesive layer, described supporting layer has the tensile strength bigger than the dry-coated bed of material.
35. laminated material according to claim 30, wherein said release liner further contains the adhesive release coat, is positioned at side liner, relative with the matsurface release coat.
36. the laminated material of claim 35 has from roll form, wherein is used to separate the required release force of the matsurface release coat and the dry-coated bed of material greater than being used for the required release force of separation gel stick release coat and formation of pressure-sensitive adhesive layer.
37. laminated material according to claim 36, wherein said adhesive layer comprises crosslinked acrylic materials.
38. a layer laminates comprises:
Comprise the dry-coated bed of material of hyaline layer and color layers, color layers comprises base-material and pigment;
Be covered in the formation of pressure-sensitive adhesive layer of color layers one side of the dry-coated bed of material; With
Be covered in the release liner on the hyaline layer, described release liner comprises thin and soft polymerization carrier film and the matsurface release coat that is made by resin-bonded agent material, described matsurface release coat contains roughening agent and described matsurface release coat and adheres on the carrier film and adhere to hyaline layer releasedly, described matsurface release coat material is cured into the sclerosis attitude on carrier film, the roughening agent that wherein is included in the release coat material forms rough surface, make that working as adhesive layer at room temperature adheres to substrate, and when release liner is peeled off from it, the rough surface facing transferred on the hyaline layer and
Therein, transfer to the level of the glossiness of hyaline layer, under 85 degree, less than 30% from the matsurface release coat.
39. according to the described laminated material of claim 38, wherein said hyaline layer comprises acrylic materials, the base-material that is contained in the color coating comprises the vinyl material.
40. a layer laminates comprises:
The dry-coated bed of material that comprises base-material and pigment, the described dry-coated bed of material has upper surface and lower surface;
Cover the dry-pressing sensitive adhesive layer of dry-coated bed of material upper surface; With
Cover the release liner of dry-coated bed of material lower surface, described release liner has the matsurface release coat that is made by resin material, resin material had been applied to already and had been cured into the sclerosis attitude on the liner and on liner, wherein the release coat material hardens with its curing, and attitude forms and the rough surface of little roughening that carrier film is isolated, when when removing release liner, rough surface is transferred to the rough surface facing on the dry-coated bed of material.
41. according to the described laminated material of claim 40, wherein from the matsurface release coat transfer to the dry-coated bed of material glossiness level 85 the degree under less than 30%.
42. according to the described laminated material of claim 40, wherein said release liner further contains the adhesive release coat, be positioned at liner a side, with matsurface release coat opposite position.
43. the laminated material of claim 42 has from roll form, wherein is used for separating the required release force of release coat greater than being used for the required release force of separation gel stick release coat from the adhesive layer from the dry-coated bed of material.
44. according to the described laminated material of claim 40, wherein said matsurface release coat material is made up of crosslinked acrylic acid modified alkyd resin and vinyl material and discrete particles material substantially.
45. a layer laminates comprises:
Have flexible polymer carrier film and the release liner that is bonded to the matsurface release coat on the carrier film, the flexible dry pigment transfer layer that adheres to the matsurface release coat releasedly, with be bonded to dry-coated material transfer layer on, the dry-pressing sensitive adhesive layer of a relative side with release liner, described dry-coated material transfer layer contains color layers, color layers comprises the pigment that is included in the polymer base material
The matsurface release coat has the adherence of certain level, and when adhesive one side of placing the dry-coated bed of material contacted with substrate, the matsurface release coat preferentially adhered to release liner to dry-coated material transfer layer, is enough to provide for the dry-coated bed of material support structure of certain level,
The matsurface release coat comprises the resin material that contains the discrete particles material, wherein said matsurface release coat material is hardened or is solidified, so that described particle forms little roughened surface, make when release coat and the dry-coated bed of material disengage, the rough surface facing is transferred on the exposed surface of the dry-coated bed of material, the gloss level that the coarse even facing that shifts has under 85 degree is less than 30%
Adhesive layer at room temperature has downtrod initial tack, this makes after the dry-coated bed of material removes release liner, allow that laminated material adheres in the substrate, adhesive layer is owing to the bonding accumulation of experiencing time lapse subsequently, makes that the dry-coated bed of material and substrate are permanent to be combined.
46. according to the described laminated material of claim 45, wherein said release liner further contains the adhesive release coat, is positioned at side liner, relative with the matsurface release coat.
47. according to the described laminated material of claim 46, have, wherein be used for separating the required release force of release coat greater than being used for the required release force of separation gel stick release coat from the adhesive layer from the dry-coated bed of material from roll form.
48. according to the described laminated material of claim 45,46 or 47, wherein formation of pressure-sensitive adhesive layer comprises the crosslinked acrylic resin material.
49. according to the described laminated material of claim 45, it comprises strengthens the polymer support layer, between the dry-coated bed of material and adhesive layer, the tensile strength that described supporting layer has is greater than the dry-coated bed of material.
50. layer laminates, comprise and be used for inner use, the dry-coated bed of material that comprises base-material and pigment, one of being positioned at the dry-coated bed of material is lip-deep, be used to adhere to the formation of pressure-sensitive adhesive layer of the dry-coated bed of material to the wall, be positioned at dry-coated bed of material surface, the release liner relative with adhesive layer, described release liner can remove time from the dry-coated bed of material after the dry-coated bed of material and wall adhere to by formation of pressure-sensitive adhesive layer, the described dry-coated bed of material has coarse facing at its exposed surface, it is characterized in that: release liner comprises on thin and soft polymerization carrier film and the carrier film, prepare by thermosetting resin, and matsurface release coat with the carrier film bonding, and form the rough surface of little roughening, make that working as adhesive layer is at room temperature sticked on the wall, and when the dry-coated bed of material removes release liner, the rough surface facing is transferred to the dry-coated bed of material, and the gloss level under 85 degree is less than 30%.
51. according to the described laminated material of claim 50, it is characterized in that: little roughened surface is to be formed by the discrete particles shape material that is included in the matsurface release coat.
52. according to the described laminated material of claim 50, it is characterized in that: described adhesive at room temperature has downtrod initial tack level, and in time through the bonding enhancing of experience, until forming permanent the combination with wall.
53. according to the described laminated material of claim 50, it is characterized in that: formation of pressure-sensitive adhesive layer comprises crosslinked acrylic materials.
54. dry-coated material transfer laminate that carries out inner use as the wall surfacing material, comprise the dry-coated bed of material that adheres to releasedly on the release liner that provides support for the dry-coated bed of material, with be positioned on the dry-coated bed of material, be in a side relative with the release liner position, be used for dope layer is adhered to formation of pressure-sensitive adhesive layer on the interior wall, wherein said release liner has release coat, this release coat can remove and makes the inside metope finishing material that the dry-coated bed of material exposes becomes colouring from the dry-coated bed of material, and, wherein said release liner is in a side of liner, on the position relative, has the adhesive release coat that contacts with the dry-coated bed of material with release coat, be characterised in that: release liner comprises the release coat on polymerization carrier film and the carrier film, described release coat comprises and being bonded on the carrier film, and the matsurface release coat that contacts with the dry-coated bed of material, described matsurface release coat is by at sclerosis forms under the attitude and carrier film is separated by little roughened surface, and has certain fusible material preparation, it can adhere to release liner on the dry-coated bed of material, but ought be at room temperature, adhere to laminated material to wall at adhesive layer, when release liner and the dry-coated bed of material disengage, again coarse facing is transferred on the exposed surface of the dry-coated bed of material, and, described laminated material has from roll form, wherein be used for separating the required release force of matsurface release coat greater than being used for the required release force of separation gel stick release coat from the formation of pressure-sensitive adhesive layer from the dry-coated bed of material, described matsurface release coat has the release force of certain level, be enough to remove liner and transferring rough surface to the dry-coated bed of material, keep dry-coated bed of material integrality on the wall simultaneously, and it is discharged from the coherent condition of it and wall.
55. according to the described laminated material of claim 54, it is characterized in that: little roughened surface is formed by the discrete particles material that is included in the matsurface releasing layer.
56. according to the described laminated material of claim 54, it is characterized in that: the level that is transferred to the glossiness of the dry-coated bed of material from the matsurface release coat is spent less than 30% 85.
57. according to the described laminated material of claim 54, it is characterized in that: formation of pressure-sensitive adhesive layer comprises internally crosslinked acrylic emulsion.
58. one kind prepares the method that the dry-coated bed of material is pressed material, comprising:
One or more decorative coating layers of coating on a side of release liner, and decorative coating individual layer or plural layer on dry or the curing release liner, on liner, to form the dry-coated bed of material, the described dry-coated bed of material comprises color layers, color layers comprises base-material and pigment, the described dry-coated bed of material has upper surface and lower surface, described release liner has the matsurface release coat that comprises resinoid bond and discrete particles, form the matsurface release surface thereon, the lower surface of the described dry-coated bed of material covers the coarse release surface of release liner and is in contact with it releasedly; With
The coating formation of pressure-sensitive adhesive layer is to the upper surface of dope layer, and described formation of pressure-sensitive adhesive layer adheres to the dry-coated bed of material on the substrate surface on applying pressure to release liner the time adaptively,
Release liner is can be from being discharged by the dry-coated bed of material that adhered to, when release liner and the dry-coated bed of material disengage, is used for coarse facing is transferred to from coarse release surface the exposed surface of dry-coated material transfer layer.
59. the method for claim 58, wherein said release liner comprises: the backing pad with upper surface and lower surface; Wherein, the matsurface release coat covers the upper surface of backing pad; Outer release coat with the lower surface that covers the backing pad; Laminated material in roll form, outer release coat contacts with formation of pressure-sensitive adhesive layer.
60. method that is used to prepare layer laminates, comprise that the applying coatings layer is to release liner, and the dope layer on dry or the curing release liner is so that form the dry-coated bed of material, described release liner comprises thin and soft polymerization carrier film, described dope layer comprises the color layers that comprises base-material and pigment, and described release liner has the release surface that contacts with the dry-coated bed of material; With the coating formation of pressure-sensitive adhesive layer to dope layer, on the side relative with release liner, be characterised in that following step: coating matsurface release coat is to release liner, described matsurface release coat at room temperature is the sclerosis attitude, prepare by resin material, has the rough surface of being separated by with carrier film, and the applying coatings layer is to rough surface and dry or solidify dope layer on the rough surface, described matsurface release coat material provides rough surface to arrive the bonding force of the dry-coated bed of material, and at room temperature can from the contact condition of the dry-coated bed of material discharge, make and to pass through formation of pressure-sensitive adhesive layer when bonding when the dry-coated bed of material and substrate surface, the rough surface facing is transferred to the exposed surface of the dry-coated bed of material, and the rough surface facing has the glossiness less than 30% under 85 degree.
61. method that is used to prepare layer laminates, comprise: the applying coatings layer is to release liner, and on release liner dry or coating material solidified layer, form the dry-coated bed of material, described release liner comprises thin and soft polymer carrier film, described dope layer comprises the color layers that contains base-material and pigment, and described release liner has the release surface that contacts with the dry-coated bed of material; With the coating formation of pressure-sensitive adhesive layer to the dope layer on the side relative with release liner, be characterised in that following steps: coating matsurface release coat is to release liner and dry or solidify release coat on this liner, on described liner, form rough surface, described release coat is made by the thermoset resin material with the liner bonding, this resin material contains the fine particle shape material of the dispersion that forms rough surface thereon, and the applying coatings layer is to rough surface and dry or solidify dope layer on the rough surface, when the dry-coated bed of material and substrate surface bonding and after this when dope layer removes release liner, rough surface is transferred to the rough surface facing on the dry-coated bed of material by formation of pressure-sensitive adhesive layer.
62. method that is used to prepare layer laminates, comprise that the applying coatings layer is to release liner, and on release liner dry or coating material solidified layer, form the dry-coated bed of material, described release liner comprises thin and soft polymer carrier film, described dope layer comprises the color layers that contains base-material and pigment, and described release liner has the release surface that contacts with the dry-coated bed of material; With the coating formation of pressure-sensitive adhesive layer to the dope layer on the side relative with release liner, characterization step is: coating matsurface release coat is to release liner and dry or solidify release coat on it, make matsurface release coat material to solidify the rough surface that the sclerosis attitude forms little roughening of being separated by with liner, and the dope layer that contacts with the matsurface release surface to matsurface release surface and drying or curing of applying coatings layer, described matsurface release coat comprises activated material under the room temperature, it is with the dry-coated bed of material and rough surface bonding, to support its adhesive layer on the dry-coated bed of material and the release liner, bonding and when after this removing release liner when the dry-coated bed of material and surface of bottom material simultaneously by formation of pressure-sensitive adhesive layer, the rough surface facing is transferred on the dry-coated bed of material.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/367,611 US20040161564A1 (en) | 2003-02-14 | 2003-02-14 | Dry paint transfer laminate |
US10/367,611 | 2003-02-14 | ||
US10/457,791 | 2003-06-09 | ||
US10/457,826 | 2003-06-09 | ||
US10/457,790 | 2003-06-09 |
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CN1780731A true CN1780731A (en) | 2006-05-31 |
CN100566991C CN100566991C (en) | 2009-12-09 |
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CNB200480009775XA Expired - Fee Related CN100566991C (en) | 2003-02-14 | 2004-02-11 | Dry-coated material transfer laminate |
CNA2004800049421A Pending CN1753733A (en) | 2003-02-14 | 2004-02-11 | Extrusion method of making a dry paint transfer laminate |
CNA2004800071317A Pending CN1761575A (en) | 2003-02-14 | 2004-02-13 | Differential release system for a self-wound multilayer dry paint decorative laminate having a pressure sensitive adhesive |
CNA2004800037744A Pending CN1747831A (en) | 2003-02-14 | 2004-02-13 | Decolor resistant product applicated color to the surface and decolor relieving method of the product applicated color to surface |
CNA2004800071232A Pending CN1761577A (en) | 2003-02-14 | 2004-02-13 | Multi-layer dry paint decorative laminate having discoloration prevention barrier |
CNA2004800076363A Pending CN1761579A (en) | 2003-02-14 | 2004-02-13 | Differential release system for a self-wound multilayer dry paint decorative laminate having a pressure sensitive adhesive |
CNA2004800076359A Pending CN1761578A (en) | 2003-02-14 | 2004-02-13 | Multi-layer dry paint decorative laminate having discoloration prevention barrier |
CNA2004800037759A Pending CN1756671A (en) | 2003-02-14 | 2004-02-13 | Article for being applied to a surface and method thereof |
Family Applications After (7)
Application Number | Title | Priority Date | Filing Date |
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CNA2004800049421A Pending CN1753733A (en) | 2003-02-14 | 2004-02-11 | Extrusion method of making a dry paint transfer laminate |
CNA2004800071317A Pending CN1761575A (en) | 2003-02-14 | 2004-02-13 | Differential release system for a self-wound multilayer dry paint decorative laminate having a pressure sensitive adhesive |
CNA2004800037744A Pending CN1747831A (en) | 2003-02-14 | 2004-02-13 | Decolor resistant product applicated color to the surface and decolor relieving method of the product applicated color to surface |
CNA2004800071232A Pending CN1761577A (en) | 2003-02-14 | 2004-02-13 | Multi-layer dry paint decorative laminate having discoloration prevention barrier |
CNA2004800076363A Pending CN1761579A (en) | 2003-02-14 | 2004-02-13 | Differential release system for a self-wound multilayer dry paint decorative laminate having a pressure sensitive adhesive |
CNA2004800076359A Pending CN1761578A (en) | 2003-02-14 | 2004-02-13 | Multi-layer dry paint decorative laminate having discoloration prevention barrier |
CNA2004800037759A Pending CN1756671A (en) | 2003-02-14 | 2004-02-13 | Article for being applied to a surface and method thereof |
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US (7) | US20040161564A1 (en) |
JP (1) | JP2009006713A (en) |
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Families Citing this family (95)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7316832B2 (en) * | 2001-12-20 | 2008-01-08 | The Procter & Gamble Company | Articles and methods for applying color on surfaces |
US7709070B2 (en) | 2001-12-20 | 2010-05-04 | The Procter & Gamble Company | Articles and methods for applying color on surfaces |
US20060165979A1 (en) * | 2002-12-13 | 2006-07-27 | Kinsey Von A | Articles and methods for applying color on surfaces |
MXPA05008667A (en) * | 2003-02-14 | 2006-04-07 | Avery Dennison Corp | Multi-layer dry paint decorative laminate having discoloration prevention barrier. |
US20040161564A1 (en) * | 2003-02-14 | 2004-08-19 | Truog Keith L. | Dry paint transfer laminate |
US20040247837A1 (en) * | 2003-06-09 | 2004-12-09 | Howard Enlow | Multilayer film |
US20050196607A1 (en) * | 2003-06-09 | 2005-09-08 | Shih Frank Y. | Multi-layer dry paint decorative laminate having discoloration prevention barrier |
US7332046B2 (en) * | 2003-09-26 | 2008-02-19 | Eastman Chemical Company | Methods of blocking stains on a substrate to be painted, and composites suitable for use in such methods |
ITVR20040014A1 (en) * | 2004-02-04 | 2004-05-04 | Bruno Zanella | PROCEDURE FOR OBTAINING A FILM AND / OR PLASTIC FILM, MADE CONTINUOUSLY, USABLE IN THE FINISHING WITH PRINT FOR SYNTHETIC LEATHER, OR ANY OTHER SUPPORT. |
KR101125678B1 (en) * | 2004-02-06 | 2012-03-28 | 롬 앤드 하스 일렉트로닉 머트어리얼즈, 엘.엘.씨. | Improved imaging compositions and methods |
CN1750929A (en) * | 2004-02-13 | 2006-03-22 | 宝洁公司 | Article for being applied to a surface and method thereof |
US20050266194A1 (en) * | 2004-05-29 | 2005-12-01 | Peters Daniel F | Peelable laminate and process of making the same |
US20070264457A1 (en) * | 2004-08-26 | 2007-11-15 | Kimoto Co., Ltd. | Material for Decoration |
US20060068213A1 (en) * | 2004-09-29 | 2006-03-30 | O'brien Kevin | Decorative laminate assembly with improved tie sheet and bridging agent |
PL1830790T3 (en) * | 2004-12-29 | 2018-08-31 | Avon Products, Inc. | Nail strips having a crosslinked polymer top coat |
US20060177649A1 (en) * | 2005-02-07 | 2006-08-10 | Clark Mark D | Methods of blocking stains on a substrate to be painted, and composites suitable for use in such methods |
US7758949B1 (en) | 2005-02-08 | 2010-07-20 | Sloan Donald D | Thermal reactive ink transfer system |
US20060191654A1 (en) * | 2005-02-25 | 2006-08-31 | John Theisen | Paper product and method for manufacturing |
JP2006247893A (en) * | 2005-03-08 | 2006-09-21 | Nissha Printing Co Ltd | Transfer film, decorative film, decorative product manufacturing method and decorative product |
US20060216453A1 (en) * | 2005-03-23 | 2006-09-28 | General Atomics | Durable pigmented film |
EP1749862A3 (en) * | 2005-08-05 | 2007-05-16 | Rohm and Haas Electronic Materials, L.L.C. | Peelable opaque coating and method of using the same |
EP2404729B1 (en) | 2005-10-21 | 2020-06-17 | Entrotech, Inc. | Composite articles comprising protective sheets and related methods |
US20070148358A1 (en) * | 2005-11-08 | 2007-06-28 | Worthen Industries | Apparatus and method for manufacturing surface protection film with a topcoat |
US7854985B2 (en) * | 2005-11-18 | 2010-12-21 | Soliant Llc | Decorative paint film laminate |
US20070215271A1 (en) * | 2006-03-02 | 2007-09-20 | Mcclintic Shawn A | Covering article and associated method |
JP4845614B2 (en) * | 2006-07-06 | 2011-12-28 | 日東電工株式会社 | Release liner, adhesive tape and adhesive tape roll |
US20080081142A1 (en) * | 2006-10-03 | 2008-04-03 | Zeik Douglas B | Articles and methods for applying color on surfaces |
US20090250164A1 (en) * | 2006-10-03 | 2009-10-08 | The Procter & Gamble Company | Methods of Making Articles for Applying Color on Surfaces |
US20090252937A1 (en) * | 2006-10-03 | 2009-10-08 | The Procter & Gamble Company | Articles for Applying Color on Surfaces |
DE102006047738A1 (en) * | 2006-10-06 | 2008-04-10 | Tesa Ag | Heat-activated adhesive tape, in particular for the bonding of electronic components and printed conductors |
US20080087370A1 (en) * | 2006-10-13 | 2008-04-17 | Custom Adhesive Products, Llc | Splicing Tape |
US20080108734A1 (en) * | 2006-11-03 | 2008-05-08 | Smith Dennis C | Ionomer pigmentation |
US20080176090A1 (en) * | 2006-12-19 | 2008-07-24 | Elia Andri E | Composite thermoplastic articles |
US20080176079A1 (en) * | 2006-12-19 | 2008-07-24 | Elia Andri E | Process for coating vehicle exterior parts made from thermoplastic composite articles |
US8263213B2 (en) * | 2006-12-19 | 2012-09-11 | E I Du Pont De Nemours And Company | Painted composite thermoplastic articles |
US7841146B2 (en) * | 2007-01-09 | 2010-11-30 | Henkel Ag & Co. Kgaa | Product and method for concealing joints |
FR2912153B1 (en) * | 2007-02-02 | 2009-04-17 | Bostik S A Sa | ADHESIVE COMPOSITION FOR SELF-ADHESIVE DECOLLABLE LABEL |
FR2918069B1 (en) * | 2007-06-29 | 2009-09-04 | Bostik S A Sa | HMPSA FOR SELF ADHESIVE LABEL DECOLLABLE |
EP2170985B1 (en) * | 2007-07-19 | 2019-06-19 | Imerys Talc America, Inc. | Silicone coatings, methods of making silicone coated articles and coated articles therefrom |
US20090061221A1 (en) * | 2007-08-07 | 2009-03-05 | Saint-Gobain Technical Fabrics | Composite tack film for asphaltic paving, method of paving, and process for making a composite tack film for asphaltic paving |
US10035932B2 (en) | 2007-09-25 | 2018-07-31 | Aero Advanced Paint Technology, Inc. | Paint replacement films, composites therefrom, and related methods |
JP2009166478A (en) * | 2007-12-17 | 2009-07-30 | Pilot Ink Co Ltd | Discolorable laminate |
US10981371B2 (en) | 2008-01-19 | 2021-04-20 | Entrotech, Inc. | Protected graphics and related methods |
US20090220768A1 (en) * | 2008-02-29 | 2009-09-03 | Hallmark Cards, Incorporated | Repositionable self-adhesive giftwrap |
EP2268486A2 (en) * | 2008-03-25 | 2011-01-05 | 3M Innovative Properties Company | Multilayer articles and methods of making and using the same |
US8932424B2 (en) * | 2008-03-25 | 2015-01-13 | 3M Innovative Properties Company | Paint film composites and methods of making and using the same |
US20100096062A1 (en) * | 2008-09-16 | 2010-04-22 | Serigraph, Inc. | Supported Article for Use in Decorating a Substrate |
WO2010099290A2 (en) * | 2009-02-25 | 2010-09-02 | Avery Dennison Corporation | Method for making multi-layer print media by extrusion coating |
US8367176B1 (en) * | 2009-03-13 | 2013-02-05 | Lolliprops, Inc. | Repositionable, self-adhesive wallpaper |
US20100252187A1 (en) * | 2009-04-02 | 2010-10-07 | Jonathan Javier Calderas | Methods of Making Customized Articles for Applying Color on Surfaces |
DE102009026548A1 (en) * | 2009-05-28 | 2011-03-24 | Henkel Ag & Co. Kgaa | Adhesive film or adhesive tape based on epoxides |
FR2946280B1 (en) * | 2009-06-03 | 2018-01-05 | Corso Magenta | SHEET ARTICLE FOR APPLICATION TO A WALL TO BE DECORATED, METHOD OF MANUFACTURE AND METHOD OF APPLICATION THEREOF |
JP5609340B2 (en) * | 2009-08-10 | 2014-10-22 | セイコーエプソン株式会社 | Transfer medium manufacturing method, transfer medium |
FR2950299B1 (en) * | 2009-09-22 | 2011-10-07 | Soc Nat Des Chemins De Fer Francais Sncf | DECORATIVE COATING WITH INTEGRATED ADHESIVE FOR TRANSPORT VEHICLE |
DE102010014381A1 (en) * | 2010-04-01 | 2011-10-06 | Karl Wörwag Lack- Und Farbenfabrik Gmbh & Co. Kg | Substrates with multicolored paint and their production |
US8742010B2 (en) * | 2010-04-09 | 2014-06-03 | Bayer Materialscience Llc | Two-component waterborne polyurethane coatings |
US8668967B2 (en) | 2011-03-15 | 2014-03-11 | Zoom Creative Products, Llc | Embellishment transfer delivery system |
US9421736B2 (en) | 2011-06-17 | 2016-08-23 | Sonoco Development, Inc. | Hybrid pressure sensitive adhesive |
CN102283491B (en) * | 2011-06-28 | 2013-03-13 | 廖静宜 | Production process of gel fingernail attaching decoration |
DE102011085223A1 (en) * | 2011-10-26 | 2013-05-02 | Tesa Se | Bio-based natural rubber compound and its use |
JP2013237214A (en) | 2012-05-16 | 2013-11-28 | Three M Innovative Properties Co | Decorative sheet |
JP2013244668A (en) * | 2012-05-25 | 2013-12-09 | Daikyo Seiko Ltd | Rubber molding |
CN103707585B (en) * | 2012-09-28 | 2016-11-16 | 广东华润涂料有限公司 | Multilayer laminated thing and preparation method thereof |
US9950559B2 (en) | 2012-09-28 | 2018-04-24 | Valspar Sourcing, Inc. | Multilayered laminate and process for preparing the same |
WO2014140056A1 (en) * | 2013-03-15 | 2014-09-18 | Akzo Nobel Coatings International B.V. | Dry primer film composite and use thereof |
US20140278277A1 (en) | 2013-03-15 | 2014-09-18 | Premier Protection Holdings, LLC | Protective film for automotive surfaces |
US9855781B2 (en) | 2013-07-15 | 2018-01-02 | Hewlett-Packard Development Company, L.P. | Printable medium |
CN103360570A (en) * | 2013-07-31 | 2013-10-23 | 常德市武陵金德镭射科技有限公司 | Waterborne polyurethane, preparation method therefor and waterborne transfer painting |
CN103512832B (en) * | 2013-10-09 | 2015-08-19 | 广东生益科技股份有限公司 | The method of glue flow state during detection pressing plate |
EP3502204B1 (en) * | 2014-03-21 | 2024-05-08 | Avery Dennison Corporation | Faceless labels and related systems and methods |
US9683143B2 (en) * | 2014-12-24 | 2017-06-20 | United States Gypsum Company | Joint finishing adhesive |
WO2016118293A1 (en) * | 2015-01-23 | 2016-07-28 | Hastings Jeffrey Logan | Paint tape device and methods of treating painted surfaces |
JP2017047687A (en) | 2015-09-04 | 2017-03-09 | 凸版印刷株式会社 | Decorative sheet |
US10753107B2 (en) * | 2016-04-11 | 2020-08-25 | Tremco Incorporated | Self-adhered sheet installation devices and methods of use |
IL262529B2 (en) * | 2016-05-30 | 2023-06-01 | Landa Labs 2012 Ltd | Method of manufacturing a multi-layer article |
CN106189911B (en) * | 2016-08-11 | 2019-05-28 | 苏州柯创电子材料有限公司 | A kind of High-strength adhesive tape and its preparation process |
CN106281078B (en) * | 2016-08-11 | 2019-06-25 | 苏州柯创电子材料有限公司 | A kind of compound one-faced tapes of graphite and its preparation process |
US9738796B1 (en) * | 2016-09-07 | 2017-08-22 | Usg Interiors, Llc | Acoustically transparent coating |
WO2018057379A1 (en) | 2016-09-20 | 2018-03-29 | Aero Advanced Paint Technology, Inc. | Paint film appliques with reduced defects, articles, and methods |
KR102475652B1 (en) * | 2016-11-29 | 2022-12-09 | 도판 인사츠 가부시키가이샤 | Cosmetic sheet and manufacturing method of cosmetic sheet |
CN109937143B (en) | 2017-01-17 | 2022-02-11 | 惠普发展公司,有限责任合伙企业 | Printable media |
DE102017101595B3 (en) * | 2017-01-27 | 2018-05-30 | Leonhard Kurz Stiftung & Co. Kg | Transfer film, its use and method for producing a transfer film and method for producing an injection molded article decorated with a transfer layer of a transfer film |
WO2018148163A1 (en) * | 2017-02-07 | 2018-08-16 | Shurtape Technologies, Llc | Digital printed duct tape |
US9855724B1 (en) | 2017-02-10 | 2018-01-02 | Custom Adhesive Products Llc | Splice tape with internal, interlayer separation interface |
WO2018183663A1 (en) * | 2017-03-30 | 2018-10-04 | Novelis Inc. | Surface roughening of polymer films |
JP7200675B2 (en) * | 2017-10-10 | 2023-01-10 | 東レ株式会社 | the film |
US20210016598A1 (en) * | 2017-11-28 | 2021-01-21 | Eliot I. RUBIN | Multi-layered decorative wrap and method of use of the same |
CN108656825B (en) * | 2018-05-15 | 2022-02-08 | 山东京宏智能科技股份有限公司 | Double-sided embossed PCM color coating steel plate and production process thereof |
CN109116582B (en) * | 2018-08-24 | 2020-02-18 | 上海康耐特光学有限公司 | Photochromic resin spectacle lens and method for producing same |
WO2020044247A1 (en) | 2018-08-28 | 2020-03-05 | Consorcio Comex S.A. De C.V. | Configurable coating system |
US20210221157A1 (en) * | 2020-01-21 | 2021-07-22 | Ready, Set, Co., LLC | Multiple layered print structure and apparatus for fabric or cloth |
US20210292593A1 (en) * | 2020-02-27 | 2021-09-23 | Ppg Industries Ohio, Inc. | Coating System |
CN112480796A (en) * | 2020-12-17 | 2021-03-12 | 广东花王涂料有限公司 | Woodware varnish and preparation method thereof |
WO2022169832A1 (en) * | 2021-02-02 | 2022-08-11 | Brewster Home Fashions Llc | Repositionable peel-and-stick embellished wall coverings |
CN114106619B (en) * | 2021-12-08 | 2023-03-24 | 固克节能科技股份有限公司 | Extinction slurry and preparation method and application thereof |
Family Cites Families (336)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US179372A (en) * | 1876-06-27 | Improvement in valves for brass musical instruments | ||
US92420A (en) * | 1869-07-13 | Improvement in cane-scraper | ||
US37479A (en) * | 1863-01-20 | Improvement in axles | ||
US26932A (en) * | 1860-01-24 | Richard a | ||
US126529A (en) * | 1872-05-07 | Improvement in type-wheels for printing-telegraphs | ||
US752498A (en) * | 1904-02-16 | Frederick william witte | ||
US1365715A (en) | 1919-06-09 | 1921-01-18 | Cornell Wood Products Co | Sizing composition |
US2746893A (en) * | 1952-12-03 | 1956-05-22 | Meyercord Co | Dry strip transfer |
US3152030A (en) | 1959-06-15 | 1964-10-06 | Mystik Tape Inc | Fused poly-laminate adhesive tape and method of making same |
GB967405A (en) | 1962-06-15 | 1964-08-19 | Ernest Leslie Whick | Improvements relating to an appliance for pasting and applying paper directly from the roll to ceiling or walls |
US3331729A (en) | 1963-02-14 | 1967-07-18 | Minnesota Mining & Mfg | Adhesive bonding method and product |
US3301741A (en) * | 1963-09-11 | 1967-01-31 | Minnesota Mining & Mfg | Adhesive sheet and method of making |
US3314838A (en) * | 1964-08-26 | 1967-04-18 | Minnesota Mining & Mfg | Pressure sensitive adhesives containing hollow spheroidal particles |
GB1232971A (en) | 1967-04-28 | 1971-05-26 | ||
US3900645A (en) | 1967-12-11 | 1975-08-19 | Morgan Adhesives Co | Scored adhesive laminate |
US3896249A (en) | 1968-01-19 | 1975-07-22 | Johnson Matthey Co Ltd | Self-adhesive transfers |
US3671236A (en) * | 1968-03-18 | 1972-06-20 | Minnesota Mining & Mfg | Presensitized color-proofing sheet |
US3640791A (en) * | 1969-02-19 | 1972-02-08 | Richard Rosenheim | Process of preparing and applying an improved painting device |
US3616192A (en) | 1970-02-04 | 1971-10-26 | Riegel Paper Corp | Decorative polyvinyl fluoride laminations |
US3654044A (en) * | 1970-11-10 | 1972-04-04 | Toyo Plywood Co Ltd | Decorative overlay paper covered plywood and process of manufacturing the same |
US3743086A (en) | 1971-02-05 | 1973-07-03 | Brady Co W H | Adhesive tape dispenser package |
US4037008A (en) * | 1971-05-17 | 1977-07-19 | Photo-Lith International | Transfer printing process and article |
US3741786A (en) | 1971-05-28 | 1973-06-26 | Avery Products Corp | Transfer tape having non-contiguous pressure sensitive adhesive patterns |
US3916046A (en) | 1971-09-13 | 1975-10-28 | Minnesota Mining & Mfg | Decorative adhesive laminate, for heat-pressure application to substrates |
US3666516A (en) * | 1971-10-12 | 1972-05-30 | Richard E Dunning | Hot stamp tape |
US4026648A (en) * | 1971-12-17 | 1977-05-31 | Canon Kabushiki Kaisha | Cleaning device for use in electrophotographic copying apparatus |
US3804700A (en) * | 1972-05-10 | 1974-04-16 | Rohm & Haas | Decorative laminate |
US4094690A (en) | 1972-08-07 | 1978-06-13 | Imperial Chemical Industries Limited | Liquid composition |
JPS4939997A (en) | 1972-08-26 | 1974-04-15 | ||
US3826701A (en) | 1972-10-31 | 1974-07-30 | Us Army | Controllable heat sealing process for optimum seal strength |
DE2254430A1 (en) | 1972-11-07 | 1974-05-09 | Rolf Herzog | Prefabricated lacquer films - useful for motor vehicle surfaces |
US3900644A (en) | 1973-03-20 | 1975-08-19 | United Merchants & Mfg | Heat resistant laminate |
US3907974A (en) * | 1973-11-08 | 1975-09-23 | Dennison Mfg Co | Curable decorating systems for glass or metal containers |
US3907628A (en) | 1973-12-20 | 1975-09-23 | United Merchants & Mfg | Applicator for self-adhesive sheet material |
US3969181A (en) | 1974-06-03 | 1976-07-13 | Minnesota Mining And Manufacturing Company | Transfer adhesive dispensing device |
US3933702A (en) * | 1974-07-10 | 1976-01-20 | National Starch And Chemical Corporation | Aqueous release coating compositions for pressure sensitive adhesives |
GB1493407A (en) | 1974-12-16 | 1977-11-30 | Ici Ltd | Decorative sheet material |
US4076895A (en) * | 1976-05-05 | 1978-02-28 | Champion International Corporation | Transparent multi-layered film and processes therefor |
CA1106993A (en) * | 1976-05-26 | 1981-08-11 | Martin M. Sackoff | Method for making a pressure sensitive adhesive coated laminate |
US4118541A (en) | 1976-11-03 | 1978-10-03 | Formica Corporation | Release sheet of a coated cellulose paper |
US4068033A (en) * | 1976-11-17 | 1978-01-10 | Commercial Decal, Inc. | Heat-releasable decalcomanias and adhesive composition therefor |
US4369157A (en) * | 1977-04-11 | 1983-01-18 | Dri-Print Foils, Inc. | Method of automatically decorating articles as they are in-mold formed automatically |
US4376159A (en) | 1977-05-09 | 1983-03-08 | Keuffel & Esser Company | Method of preparing matte finish color-proofing surprints |
US4248917A (en) * | 1977-07-18 | 1981-02-03 | Stauffer Chemical Company | Pressure sensitive products with decorative appearance |
US4248762A (en) * | 1977-07-18 | 1981-02-03 | Stauffer Chemical Company | Pressure sensitive products with decorative appearance |
GB2001912B (en) | 1977-08-08 | 1982-03-03 | Lake E | Wallpaper applicator |
DE2747978C3 (en) * | 1977-10-26 | 1981-06-04 | Dynamit Nobel Ag, 5210 Troisdorf | Method for producing an endless composite web |
DE2800635C2 (en) * | 1978-01-07 | 1985-03-14 | Fa. Leonhard Kurz, 8510 Fürth | Embossing foil, in particular hot stamping foil |
US4175156A (en) | 1978-05-19 | 1979-11-20 | Usm Corporation | Composite film adhesive |
DE2844397A1 (en) * | 1978-10-12 | 1980-04-30 | Basf Ag | COMPOSITE LAYERS FROM FILLED POLYOLEFINS AND A THERMOPLASTIC DECORATIVE LAYER, AND THEIR PRODUCTION AND USE |
US4258096A (en) * | 1978-11-09 | 1981-03-24 | Sheldahl, Inc. | Composite top membrane for flat panel switch arrays |
US4241129A (en) | 1978-12-15 | 1980-12-23 | The Dow Chemical Company | Delamination resistant multilayer metal/polymer composites |
US4235657A (en) | 1979-02-12 | 1980-11-25 | Kimberly Clark Corporation | Melt transfer web |
US4232077A (en) | 1979-02-22 | 1980-11-04 | Fritz Meisel | Hot-stamping film, and process and apparatus for its manufacture |
US4298647A (en) | 1979-07-16 | 1981-11-03 | Clopay Corporation | Cross-tearable decorative sheet material |
DE2948688A1 (en) | 1979-12-04 | 1981-06-11 | Heinz Cossonay-Ville Sovilla-Brulhart | INSULATED WALLPAPER |
DE3039721A1 (en) | 1980-10-21 | 1982-05-27 | Wacker-Chemie GmbH, 8000 München | METHOD FOR PRODUCING COVERS |
NL8005935A (en) * | 1980-10-29 | 1982-05-17 | Nordipa A G | TRANSFERABLE LACQUER, AND METHOD FOR MANUFACTURING THAT. |
US4396157A (en) * | 1981-03-17 | 1983-08-02 | Elstat Limited | Nozzle for spraying apparatus |
US4377050A (en) * | 1981-06-01 | 1983-03-22 | Renholts Roy J | Laminated tape for imprinting |
US4376151A (en) * | 1981-06-29 | 1983-03-08 | Moore Business Forms, Inc. | Pressure threshold adhesive |
JPS5813682A (en) | 1981-07-16 | 1983-01-26 | Nippon Carbide Ind Co Ltd | Pressure-sensitive adhesive layer |
US4517044A (en) * | 1981-11-18 | 1985-05-14 | Advanced Graphic Technology | Dry transfer decal and method of manufacture |
JPS58145490A (en) | 1982-02-19 | 1983-08-30 | Sumitomo Suriim Kk | Marking material |
US4499130A (en) * | 1982-03-01 | 1985-02-12 | Carprotec, Inc. | Temporary strippable protective laminate |
DE3364187D1 (en) | 1982-08-19 | 1986-07-24 | Minnesota Mining & Mfg | Composite decorative article |
EP0103344B1 (en) | 1982-09-07 | 1988-10-19 | Energy Sciences Inc. | Process of in-line coating and decorative layer lamination with panel board material and the like employing electron-beam irradiation, and decorated panel produced thereby |
US4650587A (en) * | 1982-09-09 | 1987-03-17 | Akzona Incorporated | Ammonia scavenger |
EP0103458A1 (en) | 1982-09-14 | 1984-03-21 | Reed International P.L.C. | Wallcoverings in roll form |
US4515877A (en) | 1982-11-27 | 1985-05-07 | Basf Aktiengesellschaft | Image-recording materials and image-recording carried out using these to produce an optical mask |
US4550683A (en) | 1984-01-23 | 1985-11-05 | Jones Wallace R | Sheet construction and method |
US4564406A (en) * | 1984-02-21 | 1986-01-14 | Solar-Kist Corporation | Method of and means for combination design transfer and application of heat reactivatable adhesive |
US4545090A (en) | 1984-09-24 | 1985-10-08 | Redmond Daniel R | Glass filled plastic hinge |
US4555441A (en) | 1985-03-06 | 1985-11-26 | Stik-Trim Industries, Incorporated | Self-adhesive wall covering or the like and method of making same |
US4650704A (en) * | 1985-03-06 | 1987-03-17 | Stik-Trim Industries, Inc. | Self-adhesive wall covering or the like and method of making same |
US4737225A (en) * | 1985-06-12 | 1988-04-12 | The D. L. Auld Company | Method of making a substrateless decorative article |
US4661182A (en) | 1985-07-31 | 1987-04-28 | Color Communications, Inc. | Method and composition for repairing minor surface damage to coated surfaces |
US4598020A (en) | 1985-08-16 | 1986-07-01 | Inmont Corporation | Automotive paint compositions containing pearlescent pigments and dyes |
JPH0626708B2 (en) | 1985-09-10 | 1994-04-13 | 関西ペイント株式会社 | Composite coating formation method |
DE3533136A1 (en) | 1985-09-17 | 1987-03-26 | Hoechst Ag | PARTITION FILM FOR THE PRODUCTION OF SURFACE-STRUCTURED, DECORATIVE LAMINATE PANELS |
DE3543777A1 (en) | 1985-12-11 | 1987-06-19 | Hammel Geb Messemer Christel | Process for producing forgery-proof discs and in particular forgery-proof disc produced according to this process for permanent attachment to the surface of a licence plate, an appliance housing or workpiece, a document or the like |
MY101876A (en) * | 1986-01-14 | 1992-02-15 | Minnesota Mining & Mfg | Composite useful for paint transfer and methods of use and preparation thereof. |
AT386564B (en) | 1986-02-18 | 1988-09-12 | Isovolta | DECORATIVE COMPOSITE FILM FOR SURFACE COATINGS, THEIR USE IN A MULTILAYER COMPOSITE, AND METHOD FOR PRODUCING SUCH A MULTI-LAYER COMPOSITE |
NO871019L (en) | 1986-03-17 | 1987-09-18 | Deltaglass Sa | LAMINATED SAFETY GLASS. |
US4919994A (en) * | 1986-04-01 | 1990-04-24 | Minnesota Mining And Manufacturing Company | Dry transfer graphics article and methods of preparation and use thereof |
US4759441A (en) | 1986-10-14 | 1988-07-26 | Leurck William J | Combination tool for use in hanging wallpaper |
US5342666A (en) * | 1986-10-28 | 1994-08-30 | Rexham Industries Corp. | Injection molded plastic article with integral weatherable pigmented film surface |
US4786537A (en) | 1986-10-30 | 1988-11-22 | Minnesota Mining And Manufacturing Company | Self-weeding dry transfer article |
GB8625997D0 (en) | 1986-10-30 | 1986-12-03 | Cotton Colne Ltd John | Manufacture of laminated elements |
US4711682A (en) | 1986-11-10 | 1987-12-08 | Christian Barbe | Wallpaper applicator devices and method for its use |
US4783354A (en) | 1986-12-15 | 1988-11-08 | Coated Sales, Inc. | Adherable, yet removable sheet material |
US6835267B1 (en) * | 1987-03-27 | 2004-12-28 | Avery Dennison Corporation | Dry paint transfer process and product |
US5707697A (en) | 1987-03-27 | 1998-01-13 | Avery Dennison Corporation | Dry paint transfer product having high DOI automotive paint coat |
GB2206843B (en) * | 1987-07-02 | 1991-03-13 | Crown Decorative Prod Ltd | Paste-the-wall wallcoverings and method of making |
US5000810A (en) * | 1987-08-10 | 1991-03-19 | Custom Laminations, Inc. | Decorative or printed laminates and methods for making same |
US4806184A (en) * | 1987-08-31 | 1989-02-21 | Shannon Brian P | Wallpaper applicator |
JPH01154740A (en) | 1987-12-11 | 1989-06-16 | Shin Etsu Chem Co Ltd | Adhesive structure |
US5135798A (en) * | 1987-12-03 | 1992-08-04 | Pelikan Aktiengesellschaft | Multilayer, flexible transfer strip |
US4871618A (en) | 1987-12-04 | 1989-10-03 | Shell Oil Company | Laminar structures prepared with polyketone structural adhesives |
US4902557A (en) * | 1988-01-25 | 1990-02-20 | E. I. Du Pont De Nemours And Company | Thermoplastic polyolefin composite structure |
US4854610A (en) | 1988-02-10 | 1989-08-08 | Bertek, Inc. | Method of making laminated articles and articles made therefrom |
US5075149A (en) | 1988-10-26 | 1991-12-24 | Owens R Larry | Molded hole repair patch and method of manufacture |
US5045569A (en) | 1988-11-30 | 1991-09-03 | Minnesota Mining And Manufacturing Company | Hollow acrylate polymer microspheres |
US5073457A (en) | 1988-12-01 | 1991-12-17 | Minnesota Mining And Manufacturing Company | Repositionable adhesive |
JPH02160536A (en) | 1988-12-14 | 1990-06-20 | Dainippon Printing Co Ltd | Manufacture of shining decorative sheet |
US5045386A (en) | 1989-02-01 | 1991-09-03 | Minnesota Mining And Manufacturing Company | Pressure-sensitive film composite having improved adhesion to plasticized vinyl substrates |
DE3905790A1 (en) | 1989-02-24 | 1990-09-06 | Bayer Ag | MULTILAYER COMPOSITE |
US5266372A (en) | 1989-04-24 | 1993-11-30 | Nitto Denko Corporation | Fixing tape |
JP2533174Y2 (en) * | 1989-04-24 | 1997-04-23 | 日東電工株式会社 | Adhesive tape for diapers |
AU598719B1 (en) | 1989-05-01 | 1990-06-28 | Gencorp Inc. | Thermoformable decorative rigid lamina for interiors of transportation vehicles |
US5084317A (en) | 1989-05-08 | 1992-01-28 | Avery Dennison Corporation | Pressure-sensitive adhesive release liner |
GB8911354D0 (en) * | 1989-05-17 | 1989-07-05 | Mono Web Ltd | Improvements relating to coating of substrates |
AU6293990A (en) | 1989-08-31 | 1991-04-08 | Juergen Eissele | Self-adhesive dry-transfer images, process for their manufacture and method of use |
US5203941A (en) * | 1989-10-19 | 1993-04-20 | Avery Dennison Corporation | Process for manufacturing plastic siding panels with outdoor weatherable embossed surfaces |
WO1991005660A1 (en) | 1989-10-19 | 1991-05-02 | Avery International Corporation | Process for manufacturing plastic siding panels with outdoor weatherable embossed surfaces |
US5192612A (en) * | 1989-10-31 | 1993-03-09 | Avery International Corporation | Positionable-repositionable pressure-sensitive adhesive |
US5141790A (en) | 1989-11-20 | 1992-08-25 | Minnesota Mining And Manufacturing Company | Repositionable pressure-sensitive adhesive tape |
US5034269A (en) | 1990-04-04 | 1991-07-23 | Wheeler Richard W | Process for the manufacture of paint-coated film and product produced therefrom |
US5244524A (en) * | 1990-04-09 | 1993-09-14 | Brother Kogyo Kabushiki Kaisha | Printing method for thermally transferring image section of print sheet to image receiving member |
US5229207A (en) | 1990-04-24 | 1993-07-20 | Minnesota Mining And Manufacturing Company | Film composite having repositionable adhesive by which it can become permanently bonded to a plasticized substrate |
JP2916211B2 (en) | 1990-05-17 | 1999-07-05 | ミネソタ マイニング アンド マニユフアクチユアリング カンパニー | Decorative material for EPDM rubber substrate |
US5114514A (en) * | 1990-05-30 | 1992-05-19 | Eastman Kodak Company | Bonding of thermoplastic sheet material to roughened substrates |
JPH04101846A (en) | 1990-08-22 | 1992-04-03 | Nippon Dekoratsukusu Kk | Decorative laminated sheet |
US5215826A (en) * | 1990-09-25 | 1993-06-01 | Rexham Industries Corp. | Surfacing film with thermoformable carrier layer |
IT1242070B (en) | 1990-10-11 | 1994-02-08 | Siv Soc Italiana Vetro | PROCEDURE FOR THE MANUFACTURE OF LAMINATED DECORATED SAFETY GLASS |
KR100228593B1 (en) | 1990-10-25 | 1999-11-01 | 스프레이그 로버트 월터 | Transfer article for forming retroreflective and colored images and marking same |
US5316843A (en) * | 1990-11-20 | 1994-05-31 | Somar Corporation | Matted film containing a matting agent consisting of an organic filler and an inorganic filler |
US5198301A (en) * | 1991-05-17 | 1993-03-30 | Minnesota Mining And Manufacturing Company | Flexible and conformable ionomeric resin based films |
US5196246A (en) * | 1991-05-17 | 1993-03-23 | Minnesota Mining And Manufacturing Company | Wall decorating system |
GB9119655D0 (en) * | 1991-09-13 | 1991-10-23 | Forbo Cp Ltd | Self-adhesive wallcoverings |
US5467794A (en) | 1991-09-24 | 1995-11-21 | Posit Plus | Collapsible shade structure |
AU666874B2 (en) | 1991-10-02 | 1996-02-29 | Fujicopian Co., Ltd. | Instrument for transferring coating film |
US5939479A (en) | 1991-11-22 | 1999-08-17 | Avery Dennison Corporation | Removable and guillotinable emulsion pressure-sensitive adhesives |
US5141584A (en) | 1991-11-27 | 1992-08-25 | Polaroid Corporation | Apparatus and method for controlling the delamination of a laminate |
US5169474A (en) | 1991-11-27 | 1992-12-08 | Polaroid Corporation | Apparatus and method for delaminating a composite laminate structure |
US5487927A (en) * | 1992-01-24 | 1996-01-30 | Revlon Consumer Products Corporation | Decorating method and products |
US5250336A (en) | 1992-02-11 | 1993-10-05 | Morgan Adhesives Company | Colored release liner |
ATE188421T1 (en) | 1992-04-29 | 2000-01-15 | Nicholas John Murray | COMPOSITES |
ES2141740T3 (en) | 1992-05-14 | 2000-04-01 | Decora Inc | SELF-ADHESIVE DECORATIVE MATERIAL FOR SURFACE COATING. |
US5490893A (en) | 1992-05-22 | 1996-02-13 | Avery Dennison Corporation | Thermoformable conductive laminate and process |
DE4219446C3 (en) | 1992-06-13 | 2001-01-18 | Wilhelm Taubert | Process for applying a decorative layer to a substrate |
JP3231086B2 (en) | 1992-06-30 | 2001-11-19 | テルモ株式会社 | Liquid separation device |
US5354588A (en) | 1992-07-13 | 1994-10-11 | Moore Business Forms, Inc. | Linerless labels with tie coat |
US5633225A (en) * | 1992-07-15 | 1997-05-27 | The Procter & Gamble Company | Detergent compositions inhibiting dye transfer |
US5308694A (en) * | 1992-07-31 | 1994-05-03 | Tarkett Ab | Barrier layer for floor and wall coverings |
JPH06129066A (en) * | 1992-10-19 | 1994-05-10 | Toyo Kasei Kk | Decorative sheet for exterior wall |
CA2084716C (en) * | 1992-11-05 | 1999-11-16 | John R. Johnson | Exterior automotive laminate with pressure-sensitive adhesive |
US5468532A (en) | 1992-12-10 | 1995-11-21 | Minnesota Mining And Manufacturing Company | Multilayer graphic article with color layer |
US5487929A (en) * | 1993-02-03 | 1996-01-30 | Borden, Inc. | Repositionable wall covering |
JP3142095B2 (en) * | 1993-02-23 | 2001-03-07 | 大日本印刷株式会社 | Method for producing suede-like decorative sheet |
DE4311200A1 (en) | 1993-04-05 | 1994-10-06 | Zweckform Buero Prod Gmbh | Decorative labels and processes for their manufacture |
US6312777B1 (en) | 1993-04-06 | 2001-11-06 | Decora Incorporated | Methods and composition for making a pressure sensitive adhesive coated laminate |
US5814402A (en) | 1993-04-20 | 1998-09-29 | Decora Incorporated | Pressure sensitive dry transfer graphics article and method of manufacture |
US5362812A (en) * | 1993-04-23 | 1994-11-08 | Minnesota Mining And Manufacturing Company | Reactive polymeric dyes |
GB2282128B (en) * | 1993-04-26 | 1997-07-16 | Pentel Kk | Tape dispenser |
US5409883A (en) | 1993-05-07 | 1995-04-25 | Minnesota Mining And Manufacturing Company | Process for the manufacture of multi-color donor elements for thermal transfer systems |
JPH079601A (en) * | 1993-06-07 | 1995-01-13 | Minnesota Mining & Mfg Co <3M> | Decorative film |
US5476901A (en) | 1993-06-24 | 1995-12-19 | The Procter & Gamble Company | Siloxane modified polyolefin copolymers |
DE4322140C1 (en) | 1993-07-02 | 1994-08-25 | Benecke Ag J H | Film or sheet based on polymers of ethylene and propylene, and the use thereof |
CA2128347C (en) | 1993-07-28 | 1998-12-08 | Akihiko Takano | Biodegradable adhesive tape and biodegradable adhesive label |
US5451440A (en) | 1993-07-30 | 1995-09-19 | American Tape Co. | Release coating for silicone pressure sensitive adhesives |
DE4330700C2 (en) * | 1993-09-10 | 1996-08-08 | Continental Ag | Vulcanettes for application to substrates made of rubber or rubber mixtures |
JPH09503735A (en) * | 1993-10-18 | 1997-04-15 | ミネソタ マイニング アンド マニュファクチャリング カンパニー | Tape dispenser |
US5866228A (en) * | 1993-11-22 | 1999-02-02 | Mitsubishi Chemical Corporation | Vacuum heat-insulator |
US5466324A (en) * | 1993-11-29 | 1995-11-14 | Polaroid Corporation | Apparatus and process for separation of laminae |
CN1116182C (en) | 1994-01-07 | 2003-07-30 | 美国3M公司 | Graphics transfer article |
AU691544B2 (en) | 1994-01-07 | 1998-05-21 | Minnesota Mining And Manufacturing Company | An electrostatic toner receptor layer of rubber modified thermoplastic |
US5523129A (en) | 1994-02-14 | 1996-06-04 | Mcgeehan-Hatch; Mary Kate | Removable scene-scapes bordered by an interchangeable window frame for decorating the walls of children's rooms |
JP3522822B2 (en) * | 1994-03-30 | 2004-04-26 | ミネソタ マイニング アンド マニュファクチャリング カンパニー | Decorative sheet having hammertone pattern and method of manufacturing decorative sheet |
US5441784A (en) * | 1994-04-04 | 1995-08-15 | Decora, Incorporated | Paper base wallcoverings |
US5665458A (en) | 1994-04-14 | 1997-09-09 | Specialty Adhesive Film Co. | Heat activated applique on pressure sensitive release paper and method of making |
US5442832A (en) | 1994-04-19 | 1995-08-22 | Tonsager; Wayne M. | Adjustable trowel |
US6086995A (en) | 1994-05-13 | 2000-07-11 | Decora North America | Self-wound self-adhesive surface covering material |
US5788796A (en) | 1994-05-20 | 1998-08-04 | Minnesota Mining And Manufacturing | Decal assembly and method of making same |
EP0688008A1 (en) | 1994-06-14 | 1995-12-20 | LINTEC Corporation | Printed label, method and apparatus for manufacturing printed labels, and method and apparatus for attaching printed labels |
US5403432A (en) * | 1994-06-20 | 1995-04-04 | Burch; Teresa G. | Suspendible wallpaper applicator |
US5985772A (en) | 1994-06-23 | 1999-11-16 | Cellresin Technologies, Llc | Packaging system comprising cellulosic web with a permeant barrier or contaminant trap |
EP0695629A3 (en) | 1994-07-12 | 1996-10-23 | Alkor Gmbh | Multilayered composite material, method for its manufacture and use of the same |
US5670014A (en) | 1994-10-18 | 1997-09-23 | Tapelicator, Inc. | Tape dispensing applicator and replaceable tape cartridge |
JP3929082B2 (en) * | 1994-12-05 | 2007-06-13 | リケンテクノス株式会社 | Decorative sheet and method for producing the same |
US5478432A (en) | 1994-12-16 | 1995-12-26 | Vester; Raita E. | Wallpaper border applicator apparatus |
US5643668A (en) | 1994-12-30 | 1997-07-01 | Minnesota Mining And Manufacturing Company | Tape for rough surfaces |
US5591290A (en) | 1995-01-23 | 1997-01-07 | Wallace Computer Services, Inc. | Method of making a laminate having variable adhesive properties |
US5544384A (en) | 1995-02-13 | 1996-08-13 | Forselius; Frank E. | Wall corner finishing tool |
US5573865A (en) | 1995-02-14 | 1996-11-12 | Minnesota Mining And Manufacturing Company | Graphics transfer article |
US5571557A (en) | 1995-05-09 | 1996-11-05 | Chartpak, Inc. | Faux glass etch product and process of preparing same |
US5750254A (en) * | 1995-06-05 | 1998-05-12 | Rsw, Inc., Specialty Tapes Division | Tape with plural adhesive zones and an automobile protection arrangement |
US5728469A (en) * | 1995-06-06 | 1998-03-17 | Avery Dennison Corporation | Block copolymer release surface for pressure sensitive adhesives |
US5968996A (en) * | 1995-06-07 | 1999-10-19 | Moore Business Forms, Inc. | Matte finished release composition, linerless labels incorporating the release compositon and method for making same |
US5750234A (en) * | 1996-06-07 | 1998-05-12 | Avery Dennison Corporation | Interior automotive laminate with thermoplastic low gloss coating |
ZA964731B (en) * | 1995-06-07 | 1997-01-07 | Avery Dennison Corp A Legal Bo | Extrusion coating process for making protective and decorative films |
US5676787A (en) | 1995-06-07 | 1997-10-14 | Borden Decorative Products, Inc. | Method for making repositionable wall covering and intermediate for same |
US6296732B1 (en) | 1995-06-07 | 2001-10-02 | Avery Dennison Corporation | Extrusion process for protective coatings for outdoor siding panels and the like |
DE29513170U1 (en) | 1995-08-16 | 1997-01-02 | Zweckform Etikettiertechnik | Adhesive label |
JPH09123693A (en) * | 1995-08-31 | 1997-05-13 | Nissha Printing Co Ltd | Transfer material and transfer matter |
JP3500240B2 (en) | 1995-10-27 | 2004-02-23 | リンテック株式会社 | Colored film |
US5795636A (en) | 1995-11-15 | 1998-08-18 | Minnesota Mining And Manufacturing Company | Positionable and repositionable adhesive article |
US5639539A (en) | 1995-11-29 | 1997-06-17 | Imperial Wallcoverings | Wall covering |
CA2246513C (en) | 1996-02-22 | 2004-04-20 | Idemitsu Petrochemical Co., Ltd. | Decorative film or sheet, and decorative material and building material made by using the same |
JPH09237045A (en) | 1996-02-29 | 1997-09-09 | Lintec Corp | Half vapor deposited label |
US5759270A (en) | 1996-02-29 | 1998-06-02 | Katsuyuki Miyazaki | Correction tape adhesiver for correcting mistyped letters |
US5985079A (en) | 1996-03-28 | 1999-11-16 | Rexam Industries Corp. | Flexible composite surfacing film and method for producing same |
AT404240B (en) | 1996-04-25 | 1998-09-25 | Isovolta | LAMINATE CONSISTING OF A BASE AND COVER LAYER AND METHOD FOR PRODUCING A DECORATIVE SURFACE ON THIS LAMINATE |
US5707482A (en) | 1996-05-16 | 1998-01-13 | Fusselman; Stephen M. | Removable highlighting tape |
US5904968A (en) * | 1996-05-24 | 1999-05-18 | Moore Business Forms, Inc. | Method of labeling blow molded articles with linerless labels |
US5919537A (en) | 1996-06-18 | 1999-07-06 | Android Industries Of Michigan, L.L.C. | Decorative films and laminated formable sheets with dual protective film layers |
JPH1016498A (en) * | 1996-07-02 | 1998-01-20 | Nissha Printing Co Ltd | Sheet with pattern |
US5721086A (en) * | 1996-07-25 | 1998-02-24 | Minnesota Mining And Manufacturing Company | Image receptor medium |
JPH1035086A (en) * | 1996-07-26 | 1998-02-10 | Dainippon Printing Co Ltd | Transfer film for patterning three-dimensional molding |
DE19635587B4 (en) | 1996-09-02 | 2005-12-08 | SOCIéTé BIC | Handheld device for transferring a film from z. B.klebendem, opaque or colored material from a wound on a supply reel carrier tape to a substrate |
US5981058A (en) * | 1996-09-13 | 1999-11-09 | Mannington Mills, Inc. | Stain blocking barrier layer |
US6461707B1 (en) | 1997-09-26 | 2002-10-08 | Avery Dennison Corporation | Faceless pressure-sensitive adhesive construction |
US6020062A (en) * | 1996-11-08 | 2000-02-01 | D.W. Wallcovering Inc. | Article having slippable adhesive |
US5981009A (en) * | 1997-01-30 | 1999-11-09 | Leonard Kurz Gmbh & Co. | Decorative film with hot melt adhesive layer |
US6413630B1 (en) | 1997-05-15 | 2002-07-02 | 3M Innovative Properties Company | Decorative film |
JP3954157B2 (en) * | 1997-05-30 | 2007-08-08 | スリーエム カンパニー | Decorative sheet and manufacturing method thereof |
JP3505673B2 (en) * | 1997-07-23 | 2004-03-08 | 株式会社トンボ鉛筆 | Applicator |
EP0894644B1 (en) * | 1997-07-31 | 2002-02-06 | Dominique Blanc-Brude | Pressure-activated adhesive sheet |
DE19735958A1 (en) | 1997-08-19 | 1999-02-25 | Basf Ag | Thermally curable aqueous binding agent containing activated carbon |
US5851931A (en) | 1997-09-03 | 1998-12-22 | Foss Manufacturing Co., Inc. | Paintable substrate of nonwoven fabric and extruded resin |
US6083616A (en) | 1997-09-19 | 2000-07-04 | Seal Products, Inc. | Nontack pressure activated adhesive |
KR100258600B1 (en) | 1997-10-06 | 2000-06-15 | 성재갑 | Melamine sheet laminated floorboard |
DE19744957C1 (en) * | 1997-10-10 | 1999-07-29 | Pritt Produktionsgesellschaft | Multi-layer, flexible correction tape |
EP1034090B1 (en) | 1997-11-12 | 2003-12-17 | Collins & Aikman Products Co. | Vibration dampening laminate |
US6194064B1 (en) * | 1997-12-03 | 2001-02-27 | Dyna-Tech Adhesive, Inc. | Pressure sensitive adhesive for decorative films with removable and repositionable properties |
US6096396A (en) | 1998-01-21 | 2000-08-01 | Rexam Industries Corp. | Decorative sheet material suitable for use as a flexible weatherable paint film or decal |
US6153283A (en) | 1998-02-11 | 2000-11-28 | Steelwood Extruding Corp. | Structure having at least one improved surface and a method of making the structure |
US6432241B1 (en) | 1998-03-13 | 2002-08-13 | 3M Innovative Properties Company | Splicing tape, splicing method and assembly comprising the splicing tape |
US6740379B1 (en) | 1998-03-13 | 2004-05-25 | 3M Innovative Properties Company | Adhesive tape for adhering inserts to a page of a magazine |
US6235363B1 (en) * | 1998-05-06 | 2001-05-22 | Avery Dennison Corporation | Composite construction containing barrier layer |
US6284183B1 (en) * | 1998-06-08 | 2001-09-04 | Avery Dennison Corporation | Thick sheet laminating process for making exterior automotive body panels |
US6221198B1 (en) * | 1998-06-09 | 2001-04-24 | 3M Innovative Properties Company | Method of stabilizing films or membranes using adhesive as a reservoir |
WO1999065680A1 (en) | 1998-06-15 | 1999-12-23 | Minnesota Mining And Manufacturing Company | Multi-component unidirectional graphic article |
US6852399B2 (en) | 1998-07-14 | 2005-02-08 | Dai Nippon Printing Co., Ltd. | Decorative material |
DE19837774A1 (en) | 1998-08-20 | 2000-02-24 | Waldemar Sturn | Colored film to touch-up slight vehicle paintwork damage carries a dry paint and an adhesive layer to be bonded over the damaged paintwork area |
US6391415B1 (en) | 1998-08-31 | 2002-05-21 | Environmental Inks And Coatings Corporation | Label system |
US6228486B1 (en) * | 1998-10-06 | 2001-05-08 | Avery Dennison Corporation | Thermal transfer laminate |
EP0993876B1 (en) | 1998-10-13 | 2004-03-03 | Bush Industries, Inc. | Process for applying a coloured decoration onto a substrate |
US6383613B1 (en) * | 1998-10-16 | 2002-05-07 | 3M Innovative Properties Company | Decorative film and method for the production of the same |
US6482488B1 (en) | 1998-10-28 | 2002-11-19 | 3M Innovative Properties Company | Repaired scratched and/or abraded transparent substrates having protective removable sheets thereon and a method of making |
US6394165B1 (en) | 1998-11-09 | 2002-05-28 | Steven M. Rader | Self-adhesive element dispenser and applicator device and method thereof |
GB2343864B (en) | 1998-11-20 | 2003-07-16 | Agra Vadeko Inc | Improved security thread and method and apparatus for applying same to a substrate |
US6432528B1 (en) | 1998-12-09 | 2002-08-13 | 3M Innovative Properties Company | Variably printed tape and system for printing and applying tape onto surfaces |
US6399193B1 (en) | 1998-12-18 | 2002-06-04 | The University Of Massachusetts Lowell | Surfacing laminate with bonded with pigmented pressure sensitive adhesive |
US6649682B1 (en) | 1998-12-22 | 2003-11-18 | Conforma Clad, Inc | Process for making wear-resistant coatings |
CA2291316A1 (en) | 1999-01-08 | 2000-07-08 | Nicholas A. Farkas | Silicone-containing low surface tension film |
CA2360761C (en) | 1999-01-25 | 2009-01-06 | 3M Innovative Properties Company | Vacuum-assisted laminator and methods of using the same |
US6152030A (en) | 1999-02-19 | 2000-11-28 | Fuqua; Rick Lee | Curing apparatus for a multi-color screen printing system |
EP1169181A2 (en) | 1999-03-19 | 2002-01-09 | 3M Innovative Properties Company | Image graphic adhesive system using a non-tacky adhesive |
US6324811B1 (en) | 1999-03-31 | 2001-12-04 | Jane S. Gauss | Covering an interior surface |
US6163951A (en) | 1999-03-31 | 2000-12-26 | Sealright Co., Inc. | Method and apparatus for lifting tabs of a laminate from a substrate |
US6193918B1 (en) * | 1999-04-09 | 2001-02-27 | The Procter & Gamble Company | High speed embossing and adhesive printing process and apparatus |
US6421052B1 (en) | 1999-04-09 | 2002-07-16 | The Procter & Gamble Company | Method of seaming and expanding amorphous patterns |
WO2000065383A1 (en) | 1999-04-21 | 2000-11-02 | Nippon Mitsubishi Oil Corporation | Optical laminate |
DE59901011D1 (en) | 1999-05-17 | 2002-04-25 | Argotec Lacksysteme Gmbh | Method of applying lacquer and decor to an object and method and device for laminating lacquer, decor and adhesive onto a film |
ITLU990012A1 (en) | 1999-05-24 | 2000-11-24 | Rotoplast Srl | PROCEDURE FOR INSERTING SOLID BODIES BETWEEN A PLASTIC FILM AND OTHER SUPPORTS (PLASTIC, CLOTH, LEATHER, ETC.) |
US6723427B1 (en) * | 1999-06-21 | 2004-04-20 | Avery Dennison Corporation | Fade printed decorative sheets and methods and apparatus for making the same |
WO2001000411A1 (en) | 1999-06-25 | 2001-01-04 | Toyo Kohan Co., Ltd. | Printing resin film for laminating high-sharpness decorative laminated sheet excellent in workability and high-sharpness decorative laminated sheet laminated with the resin films |
US6311399B1 (en) | 1999-10-05 | 2001-11-06 | 3M Innovative Properties Company | Multi-pin air release tool and method |
US6541109B1 (en) * | 1999-10-08 | 2003-04-01 | 3M Innovative Properties Company | Release coating formulation providing low adhesion release surfaces for pressure sensitive adhesives |
AU2748700A (en) | 1999-10-15 | 2001-04-30 | 3M Innovative Properties Company | Conformable multilayer films |
US6444311B1 (en) | 1999-10-19 | 2002-09-03 | Saint-Gobain Performance Plastics Corporation | Impact resistant protective multilayer film |
US6475616B1 (en) | 1999-11-30 | 2002-11-05 | 3M Innovative Properties Company | Paint replacement appliques |
US6482638B1 (en) | 1999-12-09 | 2002-11-19 | 3M Innovative Properties Company | Heat-relaxable substrates and arrays |
US6376058B1 (en) * | 1999-12-21 | 2002-04-23 | Avery Dennison Corporation | Polypropylene based compositions and films and labels formed therefrom |
US6461422B1 (en) | 2000-01-27 | 2002-10-08 | Chartpak, Inc. | Pressure sensitive ink jet media for digital printing |
US6554044B2 (en) | 2000-01-28 | 2003-04-29 | Fargo Electronics Inc. | Laminator peel-off bar |
US6379791B1 (en) * | 2000-02-08 | 2002-04-30 | 3M Innovative Properties Company | Compatibilized pressure-sensitive adhesives |
JP4404430B2 (en) | 2000-02-15 | 2010-01-27 | 新熊取谷石材株式会社 | Method of attaching a building decoration material and the attachment device |
JP3388437B2 (en) * | 2000-02-18 | 2003-03-24 | 大日本印刷株式会社 | Decorative sheet |
JP4069583B2 (en) * | 2000-03-28 | 2008-04-02 | 三菱電機株式会社 | Plasma display device |
JP3409016B2 (en) | 2000-04-14 | 2003-05-19 | 株式会社ダイフレックス | Waterproof sheet, joint structure of waterproof sheet and waterproofing construction method |
WO2001079372A2 (en) | 2000-04-17 | 2001-10-25 | Avery Dennison Corporation | Large-sized, mountable and removable sheet assembly and method therefor |
JP2001302991A (en) | 2000-04-20 | 2001-10-31 | Lintec Corp | Adhesive tape for painting |
US6630049B2 (en) | 2000-04-24 | 2003-10-07 | Avery Dennison Corporation | Adhesive articles with improved air egress and methods of making the same |
JP4566328B2 (en) | 2000-04-28 | 2010-10-20 | ロンシール工業株式会社 | Waterproof sheet and construction method |
US6520234B1 (en) * | 2000-05-23 | 2003-02-18 | 3M Innovative Properties Company | Steered vacuum-assisted laminating apparatus and methods of use |
US6706131B2 (en) * | 2000-05-23 | 2004-03-16 | 3M Innovative Properties Company | Film lamination and removal system and methods of use |
US6824638B1 (en) | 2000-07-27 | 2004-11-30 | 3M Innovative Properties Company | Graphic image film registration systems and methods |
JP2002067243A (en) | 2000-09-04 | 2002-03-05 | Dainippon Printing Co Ltd | Decorative sheet |
AU2002211431A1 (en) * | 2000-10-06 | 2002-04-15 | Imperial Home Decor Group Management, Inc. | Bleed-resistant dry-transfer wallcoverings |
JP2002113995A (en) | 2000-10-06 | 2002-04-16 | Toppan Printing Co Ltd | Decorative sheet and decorative material |
TW490373B (en) | 2000-10-23 | 2002-06-11 | Matsushita Electric Works Ltd | Laminate with a peelable top layer and method of peeling off the top layer from the laminate |
US6756095B2 (en) | 2001-01-10 | 2004-06-29 | Avery Dennison Corporation | Heat-sealable laminate |
US6984429B2 (en) * | 2001-01-12 | 2006-01-10 | 3M Innovative Properties Company | Laminate from which decorative films can be applied to a substrate |
EP1226958A1 (en) | 2001-01-25 | 2002-07-31 | Celfa AG | Image-receiving material having an adhesive layer, method for its' preparation, and its' use |
US6613411B2 (en) | 2001-01-25 | 2003-09-02 | 3M Innovative Properties Company | Conformable multi-layer sheet materials |
US20020142155A1 (en) | 2001-02-08 | 2002-10-03 | Steinberg Richard F. | Decorative substrate for removably adhering to a window and/or wall |
JP2002294181A (en) | 2001-03-21 | 2002-10-09 | Three M Innovative Properties Co | Decorative sheet |
US20020182955A1 (en) | 2001-03-29 | 2002-12-05 | Weglewski James T. | Structural bonding tapes and articles containing the same |
JP2002321328A (en) | 2001-04-04 | 2002-11-05 | Three M Innovative Properties Co | Decorative sheet |
WO2002083426A1 (en) | 2001-04-12 | 2002-10-24 | Avery Dennison Corporation | Metallized inkjet substrates and methods of making the same |
US6875800B2 (en) * | 2001-06-18 | 2005-04-05 | Ppg Industries Ohio, Inc. | Use of nanoparticulate organic pigments in paints and coatings |
JP2003025793A (en) * | 2001-07-13 | 2003-01-29 | Minoru Yoshida | Light storage transfer film |
US20030026932A1 (en) | 2001-07-30 | 2003-02-06 | Johnson John R. | Multilayer laminate |
JP2004538187A (en) | 2001-08-17 | 2004-12-24 | エーブリー デニソン コーポレイション | Topcoat compositions, substrates containing topcoats obtained from the compositions, and methods of preparing them |
US7022385B1 (en) * | 2001-10-04 | 2006-04-04 | Nucoat, Inc. | Laminated imaged recording media |
US6773653B2 (en) | 2001-10-05 | 2004-08-10 | Avery Dennison Corporation | In-mold labeling method |
US6601741B2 (en) | 2001-11-28 | 2003-08-05 | Illinois Tool Works Inc. | Laminated distribution manifold plate system |
ES2227059T3 (en) | 2001-12-07 | 2005-04-01 | 3M Innovative Properties Company | MULTI-LAYER SHEET THAT INCLUDES A POLYURETHANE PROTECTIVE COAT. |
US7316832B2 (en) | 2001-12-20 | 2008-01-08 | The Procter & Gamble Company | Articles and methods for applying color on surfaces |
US7709070B2 (en) | 2001-12-20 | 2010-05-04 | The Procter & Gamble Company | Articles and methods for applying color on surfaces |
WO2003059602A1 (en) | 2002-01-08 | 2003-07-24 | 3M Innovative Properties Company | Method of conforming a film to a surface |
US6752075B2 (en) | 2002-02-14 | 2004-06-22 | Stahls' Inc. | Screen printed fabric |
KR200280679Y1 (en) | 2002-02-16 | 2002-07-13 | 주식회사 다이아덤코리아 | Decotile ideastix sheet |
MXPA04008400A (en) | 2002-02-28 | 2004-11-26 | Solutia Inc | Embossed reflective laminates. |
AU2003220864A1 (en) | 2002-03-01 | 2003-09-16 | C.I. Kasei Company, Limited | Decorative sheet and process for producing the same |
US20030211334A1 (en) | 2002-05-07 | 2003-11-13 | Jones Kyle R. | Low gloss automotive interior laminates |
CN1655955B (en) | 2002-05-13 | 2010-06-16 | 宝洁公司 | Articles and methods for applying color on surfaces |
US6872268B2 (en) * | 2002-06-11 | 2005-03-29 | 3M Innovative Properties Company | Method of conforming an adherent film to a substrate by application of vacuum |
ES2200697B1 (en) | 2002-06-28 | 2005-01-01 | Alec Mian | PROCEDURE FOR THE MANUFACTURE OF TRANSLATED ARTISTIC PANELS AND MANUFACTURED PANELS. |
US7311956B2 (en) * | 2002-11-26 | 2007-12-25 | 3M Innovative Properties Company | Laminate and method used for applying a design to a substrate |
US20060165979A1 (en) | 2002-12-13 | 2006-07-27 | Kinsey Von A | Articles and methods for applying color on surfaces |
US6844041B2 (en) | 2002-12-27 | 2005-01-18 | Exxonmobil Oil Corporation | Clear polymeric label including delaminatable mask layer |
JP2004216573A (en) | 2003-01-09 | 2004-08-05 | Three M Innovative Properties Co | Decorative sheet and its manufacturing method |
MXPA05008667A (en) | 2003-02-14 | 2006-04-07 | Avery Dennison Corp | Multi-layer dry paint decorative laminate having discoloration prevention barrier. |
US20040161564A1 (en) | 2003-02-14 | 2004-08-19 | Truog Keith L. | Dry paint transfer laminate |
WO2004073967A2 (en) | 2003-02-14 | 2004-09-02 | Avery Dennison Corporation | Dry paint transfer laminate |
EP1594626A4 (en) | 2003-02-14 | 2008-02-20 | Avery Dennison Corp | Extrusion method of making a dry paint transfer laminate |
US20040170855A1 (en) | 2003-02-27 | 2004-09-02 | Shigeo Kawabata | Decorative film-like material and decorative sheet |
EP1462423A1 (en) | 2003-03-21 | 2004-09-29 | Cristales Curvados S.A. | Ornamental multilayer glass |
US20050196607A1 (en) | 2003-06-09 | 2005-09-08 | Shih Frank Y. | Multi-layer dry paint decorative laminate having discoloration prevention barrier |
US20040247837A1 (en) | 2003-06-09 | 2004-12-09 | Howard Enlow | Multilayer film |
US7204288B2 (en) | 2003-06-10 | 2007-04-17 | The Procter & Gamble Company | Multi-burnish applicator for and method of applying a sheet material to a substrate |
US6808586B1 (en) | 2003-06-10 | 2004-10-26 | The Procter & Gamble Company | Applicator for and method of applying a sheet material to a substrate |
AU2003245534A1 (en) | 2003-06-16 | 2005-02-04 | Serigraph Inc. | Architectural graphic system |
JP2005220337A (en) | 2004-01-09 | 2005-08-18 | Nichiban Co Ltd | Pressure-sensitive adhesive sheet, decorative sheet with surface gloss, and inkjet printing medium |
JP2005206724A (en) | 2004-01-23 | 2005-08-04 | Three M Innovative Properties Co | Decorative film |
WO2005075591A1 (en) | 2004-02-02 | 2005-08-18 | 3M Innovative Properties Company | Method of producing colored graphic marking films |
MXPA05008553A (en) * | 2004-02-13 | 2005-12-05 | Procter & Gamble | Discoloration-resistant articles for applying color on surfaces and methods of reducing discoloration in articles for applying color on surfaces. |
CN1750929A (en) * | 2004-02-13 | 2006-03-22 | 宝洁公司 | Article for being applied to a surface and method thereof |
JP2007533491A (en) | 2004-04-16 | 2007-11-22 | ミリケン・アンド・カンパニー | Textile structure |
US20050255271A1 (en) | 2004-05-11 | 2005-11-17 | Joseph Brimo | Apparently seamless wall covering system |
US20060073318A1 (en) * | 2004-10-06 | 2006-04-06 | Applied Extrusion Technologies, Inc. | Opaque decorative film and construction laminates employing same |
US20060088695A1 (en) * | 2004-10-21 | 2006-04-27 | Theodore Coburn | Multilayer separable film or sheet |
US20060093776A1 (en) * | 2004-11-03 | 2006-05-04 | Crum Jesse D | Pressure sensitive laminate assembly having faux patterned embossments for use with business communication documents and method of creating a business document |
-
2003
- 2003-02-14 US US10/367,611 patent/US20040161564A1/en not_active Abandoned
- 2003-06-09 US US10/457,791 patent/US7807246B2/en not_active Expired - Fee Related
- 2003-06-09 US US10/457,826 patent/US7132142B2/en not_active Expired - Fee Related
- 2003-06-09 US US10/457,806 patent/US20040159969A1/en not_active Abandoned
- 2003-06-09 US US10/457,790 patent/US7905981B2/en not_active Expired - Fee Related
-
2004
- 2004-02-11 CN CNB200480009775XA patent/CN100566991C/en not_active Expired - Fee Related
- 2004-02-11 CN CNA2004800049421A patent/CN1753733A/en active Pending
- 2004-02-13 CN CNA2004800071317A patent/CN1761575A/en active Pending
- 2004-02-13 CN CNA2004800037744A patent/CN1747831A/en active Pending
- 2004-02-13 CN CNA2004800071232A patent/CN1761577A/en active Pending
- 2004-02-13 CN CNA2004800076363A patent/CN1761579A/en active Pending
- 2004-02-13 CN CNA2004800076359A patent/CN1761578A/en active Pending
- 2004-02-13 CN CNA2004800037759A patent/CN1756671A/en active Pending
-
2005
- 2005-10-12 US US11/248,047 patent/US7722938B2/en not_active Expired - Fee Related
-
2006
- 2006-11-07 US US11/557,146 patent/US20070065621A1/en not_active Abandoned
-
2008
- 2008-07-02 JP JP2008173436A patent/JP2009006713A/en active Pending
Also Published As
Publication number | Publication date |
---|---|
CN100566991C (en) | 2009-12-09 |
US7132142B2 (en) | 2006-11-07 |
CN1747831A (en) | 2006-03-15 |
CN1761577A (en) | 2006-04-19 |
US7905981B2 (en) | 2011-03-15 |
US20070065621A1 (en) | 2007-03-22 |
US20040159969A1 (en) | 2004-08-19 |
CN1761575A (en) | 2006-04-19 |
CN1756671A (en) | 2006-04-05 |
JP2009006713A (en) | 2009-01-15 |
US20060029765A1 (en) | 2006-02-09 |
US20040161568A1 (en) | 2004-08-19 |
CN1753733A (en) | 2006-03-29 |
US7807246B2 (en) | 2010-10-05 |
US20040161567A1 (en) | 2004-08-19 |
CN1761579A (en) | 2006-04-19 |
US20040161564A1 (en) | 2004-08-19 |
US7722938B2 (en) | 2010-05-25 |
US20040161566A1 (en) | 2004-08-19 |
CN1761578A (en) | 2006-04-19 |
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